Canonical Allele Identifier: CA255082278

Gene:

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.94811138C>A , CM000675.2:g.94811138C>A	GRCh38
NC_000013.10:g.95463392C>A , CM000675.1:g.95463392C>A	GRCh37
NC_000013.9:g.94261393C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110754.1:n.256+46587C>A