Canonical Allele Identifier: CA1689217957

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400486C= , CM000669.2:g.13400486C=	GRCh38
NC_000007.13:g.13440111C= , CM000669.1:g.13440111C=	GRCh37
NC_000007.12:g.13406636C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90163C=