| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.640843C= , CM000686.2:g.640843C= | GRCh38 |
| NC_000024.9:g.551578C= , CM000686.1:g.551578C= | GRCh37 |
| NC_000024.8:g.521578C= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000711141.1:c.509C= | ENSP00000518639.1:p.Ala170= |
| ENST00000711142.1:c.509C= | ENSP00000518640.1:p.Ala170= |
| ENST00000711143.1:c.509C= | ENSP00000518641.1:p.Ala170= |
| ENST00000711145.1:c.509C= | ENSP00000518642.1:p.Ala170= |