Canonical Allele Identifier: CA1139789788

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.213424498T= , CM000663.2:g.213424498T=	GRCh38
NC_000001.10:g.213597841T= , CM000663.1:g.213597841T=	GRCh37
NC_000001.9:g.211664464T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001738463.1:n.260+24189T=