Canonical Allele Identifier: CA2381739216

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.22259427T= , CM000683.2:g.22259427T=	GRCh38
NC_000021.8:g.23631747T= , CM000683.1:g.23631747T=	GRCh37
NC_000021.7:g.22553618T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754978.1:n.221+46614T=