Canonical Allele Identifier: CA910080613

Gene:

Linked Data

• dbSNP Id: rs1401373034
• MyVariant Identifiers: chr3:g.72315989A>G (hg19) ; chr3:g.72266838A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266838A>G , CM000665.2:g.72266838A>G	GRCh38
NC_000003.11:g.72315989A>G , CM000665.1:g.72315989A>G	GRCh37
NC_000003.10:g.72398679A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8270T>C