Canonical Allele Identifier: CA1732290218

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.106718770C= , CM000669.2:g.106718770C=	GRCh38
NC_000007.13:g.106359216C= , CM000669.1:g.106359216C=	GRCh37
NC_000007.12:g.106146452C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745317.1:n.119+13572G=