| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108578292del , CM000685.2:g.108578292del | GRCh38 |
| NC_000023.10:g.107821522del , CM000685.1:g.107821522del | GRCh37 |
| NC_000023.9:g.107708178del | NCBI36 |
| NG_011977.1:g.143369del | |
| NG_011977.2:g.143369del |
| HGVS | Amino-acid Change |
|---|---|
| NM_000495.4:c.689del | |
| NM_000495.5:c.689del | |
| NM_033380.2:c.689del | |
| NM_033380.3:c.689del | |
| ENST00000328300.10:c.689del | |
| ENST00000328300.11:c.689del | |
| ENST00000361603.6:c.689del | |
| ENST00000361603.7:c.689del | |
| XM_005262070.2:c.689del | |
| XM_005262072.3:c.689del | |
| XM_006724616.2:c.689del | |
| XM_011530849.1:c.365del | |
| XM_011530849.2:c.704del | |
| XM_011530850.1:c.689del | |
| XM_017029259.2:c.704del | |
| XM_017029260.1:c.704del | |
| XM_017029261.1:c.704del | |
| XM_017029262.2:c.704del |