Canonical Allele Identifier: CA965996494
Gene:

Linked Data

dbSNP Id: rs1884676015

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314750G>A , CM000676.2:g.92314750G>A GRCh38
NC_000014.8:g.92781094G>A , CM000676.1:g.92781094G>A GRCh37
NC_000014.7:g.91850847G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-496G>A