Canonical Allele Identifier: CA2263926987

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211864C= , CM000679.2:g.50211864C=	GRCh38
NC_000017.10:g.48289225C= , CM000679.1:g.48289225C=	GRCh37
NC_000017.9:g.45644224C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-1971C=