Canonical Allele Identifier: CA1649517548

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98136857C= , CM000668.2:g.98136857C=	GRCh38
NC_000006.11:g.98584733C= , CM000668.1:g.98584733C=	GRCh37
NC_000006.10:g.98691454C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942809.1:n.456+37587C=