Canonical Allele Identifier: CA2381739145

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.22259300T= , CM000683.2:g.22259300T=	GRCh38
NC_000021.8:g.23631620T= , CM000683.1:g.23631620T=	GRCh37
NC_000021.7:g.22553491T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754978.1:n.221+46487T=