Canonical Allele Identifier: CA656467457

Gene:

Linked Data

• dbSNP Id: rs2141995005
• COSMIC: COSN25004030

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419418G>A , CM000677.2:g.87419418G>A	GRCh38
NC_000015.9:g.87962649G>A , CM000677.1:g.87962649G>A	GRCh37
NC_000015.8:g.85763653G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-147C>T
XR_932585.1:n.340-147C>T
XR_001751647.1:n.617-147C>T
XR_932585.2:n.627-147C>T