Canonical Allele Identifier: CA10576203

Gene:

Identifiers and link-outs to other resources

• ClinVar Variation Id: 225986
• ClinVar RCV Id: RCV000211200 ; RCV000211227 ; RCV000211287 ; RCV000211288 ; RCV000211383 ; RCV000211411
• dbSNP Id: rs2952768
• gnomAD: 2:208494234 T / C
• MyVariant Identifiers: chr2:g.208494234T>C (hg19) ; chr2:g.207629510T>C (hg38)
• PubMed: PMID:22992668 ; PMID:23183491 ; PMID:25615449

User contributed link-outs

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.207629510T>C , CM000664.2:g.207629510T>C	GRCh38
NC_000002.11:g.208494234T>C , CM000664.1:g.208494234T>C	GRCh37
NC_000002.10:g.208202479T>C	NCBI36