Canonical Allele Identifier: CA651407361

Gene:

Linked Data

• COSMIC: COSN20613843

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812589T>C , CM000668.2:g.155812589T>C	GRCh38
NC_000006.11:g.156133723T>C , CM000668.1:g.156133723T>C	GRCh37
NC_000006.10:g.156175415T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19170T>C
XR_943146.1:n.645-550A>G
XR_001744423.1:n.699-550A>G
XR_001744424.1:n.79+19170T>C