Canonical Allele Identifier: CA1857743752

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78468981G= , CM000671.2:g.78468981G=	GRCh38
NC_000009.11:g.81083897G= , CM000671.1:g.81083897G=	GRCh37
NC_000009.10:g.80273717G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746759.1:n.3871G=