Canonical Allele Identifier:
CA2255112015
Gene:
Linked Data
dbSNP Id:
rs1567826486
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237323G>T , CM000679.2:g.30237323G>T | GRCh38 |
| NC_000017.10:g.28564341G>T , CM000679.1:g.28564341G>T | GRCh37 |
| NC_000017.9:g.25588467G>T | NCBI36 |
| NG_011747.2:g.3614C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.165+253G>T | ||
| XR_001752824.1:n.280+253G>T |