Canonical Allele Identifier: CA1796404063

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191132T= , CM000670.2:g.79191132T=	GRCh38
NC_000008.10:g.80103367T= , CM000670.1:g.80103367T=	GRCh37
NC_000008.9:g.80265922T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745720.1:n.105+761T=