Canonical Allele Identifier:
CA2129379016
Gene:
Linked Data
dbSNP Id:
rs1882059547
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36384761T>A , CM000676.2:g.36384761T>A | GRCh38 |
| NC_000014.8:g.36853966T>A , CM000676.1:g.36853966T>A | GRCh37 |
| NC_000014.7:g.35923717T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537428.1:c.319-12398T>A | XP_011535730.1:n.319-12398T>A | |
| XR_943756.1:n.358+23665T>A |