Canonical Allele Identifier: CA653585449

Gene:

Linked Data

• dbSNP Id: rs4986894
• COSMIC: COSN8863080

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762608T>G , CM000672.2:g.94762608T>G	GRCh38
NC_000010.10:g.96522365T>G , CM000672.1:g.96522365T>G	GRCh37
NC_000010.9:g.96512355T>G	NCBI36
NG_008384.2:g.4903T>G
NG_008384.3:g.4928T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000464755.1:c.932-12450T>G	ENSP00000483243.1:n.932-12450T>G