Canonical Allele Identifier: CA1573933722

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113661089C= , CM000667.2:g.113661089C=	GRCh38
NC_000005.9:g.112996786C= , CM000667.1:g.112996786C=	GRCh37
NC_000005.8:g.113024685C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742841.1:n.59+27725C=