Canonical Allele Identifier:
CA2255111941
Gene:
Linked Data
dbSNP Id:
rs1907317556
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237265_30237267del , CM000679.2:g.30237265_30237267del | GRCh38 |
| NC_000017.10:g.28564283_28564285del , CM000679.1:g.28564283_28564285del | GRCh37 |
| NC_000017.9:g.25588409_25588411del | NCBI36 |
| NG_011747.2:g.3671_3673del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.165+195_165+197del | ||
| XR_001752824.1:n.280+195_280+197del |