Canonical Allele Identifier: CA906314285

Gene:

Linked Data

• dbSNP Id: rs9874556
• gnomAD v3: 3-3314490-A-T
• gnomAD v4: 3-3314490-A-T
• MyVariant Identifiers: chr3:g.3356174A>T (hg19) ; chr3:g.3314490A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3314490A>T , CM000665.2:g.3314490A>T	GRCh38
NC_000003.11:g.3356174A>T , CM000665.1:g.3356174A>T	GRCh37
NC_000003.10:g.3331174A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_940546.1:n.337+22810T>A