Canonical Allele Identifier: CA2096716580

Gene:

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.62862667A>C , CM000675.2:g.62862667A>C	GRCh38
NC_000013.10:g.63436800A>C , CM000675.1:g.63436800A>C	GRCh37
NC_000013.9:g.62334801A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942013.1:n.292-23414T>G