Canonical Allele Identifier: CA2581165212
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384931C>A , CM000676.2:g.36384931C>A GRCh38
NC_000014.8:g.36854136C>A , CM000676.1:g.36854136C>A GRCh37
NC_000014.7:g.35923887C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12228C>A XP_011535730.1:n.319-12228C>A
XR_943756.1:n.358+23835C>A