Canonical Allele Identifier: CA651407362

Gene:

Linked Data

• dbSNP Id: rs1778858923
• gnomAD v3: 6-155812679-A-G
• gnomAD v4: 6-155812679-A-G
• COSMIC: COSN22351310

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812679A>G , CM000668.2:g.155812679A>G	GRCh38
NC_000006.11:g.156133813A>G , CM000668.1:g.156133813A>G	GRCh37
NC_000006.10:g.156175505A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19260A>G
XR_943146.1:n.645-640T>C
XR_001744423.1:n.699-640T>C
XR_001744424.1:n.79+19260A>G