Canonical Allele Identifier: CA2383342512

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25454202T= , CM000683.2:g.25454202T=	GRCh38
NC_000021.8:g.26826514T= , CM000683.1:g.26826514T=	GRCh37
NC_000021.7:g.25748385T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_937615.1:n.78-776A=