Canonical Allele Identifier: CA1641143550

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80593088C= , CM000668.2:g.80593088C=	GRCh38
NC_000006.11:g.81302805C= , CM000668.1:g.81302805C=	GRCh37
NC_000006.10:g.81359524C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002956360.1:n.182+12683C=