Canonical Allele Identifier: CA344464

Gene:

Linked Data

• ClinVar Variation Id: 41400
• ClinVar RCV Id: RCV000034302
• dbSNP Id: rs199422256
• MyVariant Identifiers: chr3:g.169482948G>C (hg19) ; chr3:g.169765160G>C (hg38)
• PubMed: PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765160G>C , CM000665.2:g.169765160G>C	GRCh38
NC_000003.11:g.169482948G>C , CM000665.1:g.169482948G>C	GRCh37
NC_000003.10:g.170965642G>C	NCBI36
NG_016363.1:g.4901C>G , LRG_347:g.4901C>G