Canonical Allele Identifier: CA656442273

Gene:

Linked Data

• dbSNP Id: rs1898216949
• COSMIC: COSN22390165

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249677C>T , CM000678.2:g.9249677C>T	GRCh38
NC_000016.9:g.9343534C>T , CM000678.1:g.9343534C>T	GRCh37
NC_000016.8:g.9251035C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64944C>T