Canonical Allele Identifier: CA1692752230

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20007952A= , CM000669.2:g.20007952A=	GRCh38
NC_000007.13:g.20047575A= , CM000669.1:g.20047575A=	GRCh37
NC_000007.12:g.20014100A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110114.1:n.210+20967T=