Canonical Allele Identifier: CA1139908707

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94586920G= , CM000663.2:g.94586920G=	GRCh38
NC_000001.10:g.95052476G= , CM000663.1:g.95052476G=	GRCh37
NC_000001.9:g.94825064G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001738161.1:n.461+23307G=