Canonical Allele Identifier: CA166591526

Gene:

Linked Data

• dbSNP Id: rs760136767
• gnomAD v3: 7-124306173-A-G
• gnomAD v4: 7-124306173-A-G
• MyVariant Identifiers: chr7:g.123946227A>G (hg19) ; chr7:g.124306173A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306173A>G , CM000669.2:g.124306173A>G	GRCh38
NC_000007.13:g.123946227A>G , CM000669.1:g.123946227A>G	GRCh37
NC_000007.12:g.123733463A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002956584.1:n.73-305A>G