Canonical Allele Identifier: CA2263926971

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211835T= , CM000679.2:g.50211835T=	GRCh38
NC_000017.10:g.48289196T= , CM000679.1:g.48289196T=	GRCh37
NC_000017.9:g.45644195T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-2000T=