Canonical Allele Identifier: CA1140002113

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.4608610G= , CM000663.2:g.4608610G=	GRCh38
NC_000001.10:g.4668670G= , CM000663.1:g.4668670G=	GRCh37
NC_000001.9:g.4568530G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001737775.1:n.489+567G=