Skip to content

rCRS

Definition

The revised Cambridge Reference Sequence (GenBank accession NC_012920), the standard reference for human mitochondrial DNA. All mtDNA variant positions in forensic and clinical reports are numbered relative to the rCRS. It replaced the original Cambridge Reference Sequence (cRS) in 1999 after resequencing identified a small number of errors and an A-to-C change at position 263.

Length
16,569 base pairs
GenBank Accession
NC_012920
Adopted
1999
Required By
ISFG, ENFSI, and EMPOP standards

Common questions

What is rCRS and why do forensic labs use it?+

rCRS is the Revised Cambridge Reference Sequence, the standard 16,569-base-pair human mitochondrial DNA sequence adopted in 1999. Forensic labs use it as a universal benchmark so that when they find a mtDNA variant, they can report it as a difference from rCRS positions. This standardization across labs makes results comparable and reproducible.

How is rCRS different from the original Cambridge Reference Sequence?+

The rCRS replaced the original 1981 Anderson sequence after resequencing in 1999 found errors and an A-to-C change at position 263. It corrected those mistakes and is now the mandatory reference for forensic and clinical mtDNA reporting under international standards like ISFG and ENFSI.

What does it mean when a forensic report says 'differences from rCRS'?+

Instead of listing the entire mtDNA sequence, labs report only the positions where the person's mtDNA differs from the rCRS template. For each difference, they note the position number and the base found there. This makes reports concise and standardized across all forensic cases.

Related terms

Heteroplasmy
The co-existence of two or more mitochondrial DNA sequence variants within a single individual, arising from somatic mutation or incomplete segregation. Length...
AFDIL
Armed Forces DNA Identification Laboratory, at Dover Air Force Base, Delaware. The US military's central identification laboratory, responsible for mtDNA-based identification of...
D-Loop
The non-coding displacement-loop control region of the mitochondrial genome (~bp 16024-576 in the rCRS). Contains the origin of replication and the promoters,...
E-Value (BLAST)
The expected number of alignments as good as the query result that would occur by chance in a database of the given...
EMPOP
EMPOP mtDNA Population Database, maintained at the Institute of Legal Medicine, Innsbruck, Austria. Contains over 50,000 curated mtDNA sequences and uses phylogenetic...
EMPOP SAM2
The submission quality-assurance module used by the EMPOP database to screen incoming mtDNA sequences for phylogenetic inconsistencies, sequencing artefacts, and nomenclature errors....
Haplogroup
A monophyletic branch of the human mitochondrial (or Y-chromosome) phylogenetic tree defined by a set of derived mutations. Haplogroup assignment is the...
Hypervariable Region (HV1, HV2)
Two segments within the mitochondrial D-loop that accumulate sequence variation faster than the coding mitochondrial genome. HV1 spans positions 16024-16365; HV2 spans...
INSDC
International Nucleotide Sequence Database Collaboration, the three-way partnership between GenBank (NCBI/NLM, US), ENA (EMBL-EBI, UK/EU), and DDBJ (National Institute of Genetics, Japan)...
Petrous Bone
The petrous portion of the temporal bone, the densest bone in the human skull. Its dense hydroxyapatite matrix protects enclosed DNA from...
Protamine
Small arginine-rich proteins that replace histones in the nuclei of spermatozoa during spermatogenesis, producing a hyper-compacted chromatin structure approximately six times denser...
RSRS
Reconstructed Sapiens Reference Sequence (2012). A phylogenetically derived ancestral human mtDNA sequence used in academic population genetics but not in forensic casework...

Explained in these topics

Your journey to becoming a forensic professional starts here.

Practice with mock tests, learn from structured notes, and get your questions answered by a global forensic community, all in one place.