Canonical Allele Identifier: CA2293960168

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756731T= , CM000680.2:g.31756731T=	GRCh38
NC_000018.9:g.29336694T= , CM000680.1:g.29336694T=	GRCh37
NC_000018.8:g.27590692T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5408T=