| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508976del , CM000685.2:g.83508976del | GRCh38 |
| NC_000023.10:g.82763984del , CM000685.1:g.82763984del | GRCh37 |
| NC_000023.9:g.82650640del | NCBI36 |
| NG_009936.2:g.5716del |
| HGVS | Amino-acid Change |
|---|---|
| NM_000307.5:c.652del MANE Select | NP_000298.3:p.Ala218ArgfsTer23 |
| ENST00000644024.2:c.652del MANE Select | ENSP00000495996.1:p.Ala218ArgfsTer23 |
| NM_000307.4:c.652del | NP_000298.3:p.Ala218ArgfsTer23 |
| ENST00000373200.4:c.652del | ENSP00000362296.2:p.Ala218ArgfsTer23 |