Canonical Allele Identifier: CA653477961

Gene:

Linked Data

• COSMIC: COSN20903582 ; COSN24165894

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697399C>T , CM000672.2:g.8697399C>T	GRCh38
NC_000010.10:g.8739362C>T , CM000672.1:g.8739362C>T	GRCh37
NC_000010.9:g.8779368C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27598G>A