Linked Data
dbSNP Id:
rs2097503428
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122507181del , CM000672.2:g.122507181del | GRCh38 |
| NC_000010.10:g.124266697del , CM000672.1:g.124266697del | GRCh37 |
| NC_000010.9:g.124256687del | NCBI36 |
| NG_011554.1:g.50657del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.973-189del MANE Select | ENSP00000357980.3:n.973-189del | |
| ENST00000648167.1:c.655-189del | ENSP00000498033.1:n.655-189del | |
| ENST00000368984.7:c.973-189del | ENSP00000357980.3:n.973-189del | |
| ENST00000420892.1:c.196-189del | ENSP00000412676.1:n.196-189del | |
| NM_002775.4:c.973-189del | NP_002766.1:n.973-189del | |
| NM_002775.5:c.973-189del MANE Select | NP_002766.1:n.973-189del |