Canonical Allele Identifier: CA708251760

Gene:

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.71199580C>A , CM000676.2:g.71199580C>A	GRCh38
NC_000014.8:g.71666297C>A , CM000676.1:g.71666297C>A	GRCh37
NC_000014.7:g.70736050C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537452.2:c.888-9242G>T	XP_011535754.2:n.888-9242G>T