Canonical Allele Identifier: CA1965010309

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.38267043C= , CM000673.2:g.38267043C=	GRCh38
NC_000011.9:g.38288593C= , CM000673.1:g.38288593C=	GRCh37
NC_000011.8:g.38245169C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_931202.1:n.303+58132G=