Canonical Allele Identifier: CA1565400651

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96389909C= , CM000667.2:g.96389909C=	GRCh38
NC_000005.9:g.95725613C= , CM000667.1:g.95725613C=	GRCh37
NC_000005.8:g.95751369C=	NCBI36
NG_021161.1:g.48373G=

Transcript Alleles

HGVS	Amino-acid Change
NR_130776.1:n.354+10257C=