Canonical Allele Identifier: CA2170931653

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38614852G= , CM000677.2:g.38614852G=	GRCh38
NC_000015.9:g.38907053G= , CM000677.1:g.38907053G=	GRCh37
NC_000015.8:g.36694345G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751736.1:n.281+2397G=