Canonical Allele Identifier: CA645821902

Gene:

Linked Data

• COSMIC: COSN26501110

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.56385051C>T , CM000663.2:g.56385051C>T	GRCh38
NC_000001.10:g.56850723C>T , CM000663.1:g.56850723C>T	GRCh37
NC_000001.9:g.56623311C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641109.1:c.759+93835G>A	ENSP00000493138.1:n.759+93835G>A
ENST00000641346.1:c.366+15043G>A
ENST00000641415.1:c.192+98212G>A
ENST00000641494.1:c.378+98212G>A
ENST00000642129.1:c.768+98212G>A