Canonical Allele Identifier: CA832742515

Gene:

Linked Data

• dbSNP Id: rs7778156
• gnomAD v3: 7-124306384-T-A
• gnomAD v4: 7-124306384-T-A
• MyVariant Identifiers: chr7:g.123946438T>A (hg19) ; chr7:g.124306384T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306384T>A , CM000669.2:g.124306384T>A	GRCh38
NC_000007.13:g.123946438T>A , CM000669.1:g.123946438T>A	GRCh37
NC_000007.12:g.123733674T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002956584.1:n.73-94T>A