Canonical Allele Identifier: CA1818149162

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.126999277A= , CM000670.2:g.126999277A=	GRCh38
NC_000008.10:g.128011522A= , CM000670.1:g.128011522A=	GRCh37
NC_000008.9:g.128080704A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746076.2:n.1301-7278A=