Canonical Allele Identifier: CA2293960114

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756592T= , CM000680.2:g.31756592T=	GRCh38
NC_000018.9:g.29336555T= , CM000680.1:g.29336555T=	GRCh37
NC_000018.8:g.27590553T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5547T=