Canonical Allele Identifier: CA1140300093

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94587797T= , CM000663.2:g.94587797T=	GRCh38
NC_000001.10:g.95053353T= , CM000663.1:g.95053353T=	GRCh37
NC_000001.9:g.94825941T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001738161.1:n.461+24184T=