| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92645640G>T , CM000672.2:g.92645640G>T | GRCh38 |
| NC_000010.10:g.94405397G>T , CM000672.1:g.94405397G>T | GRCh37 |
| NC_000010.9:g.94395377G>T | NCBI36 |
| NG_032580.1:g.57573G>T |
| HGVS | Amino-acid Change |
|---|---|
| NM_004523.4:c.2545G>T MANE Select | NP_004514.2:p.Glu849Ter |
| ENST00000260731.5:c.2545G>T MANE Select | ENSP00000260731.3:p.Glu849Ter |
| NM_004523.3:c.2545G>T | NP_004514.2:p.Glu849Ter |
| ENST00000260731.4:c.2545G>T | ENSP00000260731.3:p.Glu849Ter |
| ENST00000676621.1:c.*1063G>T | ENSP00000503639.1:n.*1063G>T |
| ENST00000676647.1:c.2338G>T | ENSP00000503394.1:p.Glu780Ter |
| ENST00000676757.1:c.2338G>T | ENSP00000504289.1:p.Glu780Ter |
| ENST00000677720.1:c.*519G>T | ENSP00000504840.1:n.*519G>T |