Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97611514C= , CM000672.2:g.97611514C= | GRCh38 |
| NC_000010.10:g.99371271C= , CM000672.1:g.99371271C= | GRCh37 |
| NC_000010.9:g.99361261C= | NCBI36 |
| NG_027922.1:g.32170C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_138413.4:c.839C= MANE Select | NP_612422.2:p.Thr280= |
| ENST00000370646.9:c.839C= MANE Select | ENSP00000359680.4:p.Thr280= |
| NM_001134670.1:c.350C= | NP_001128142.1:p.Thr117= |
| NM_001134670.2:c.350C= | NP_001128142.1:p.Thr117= |
| NM_138413.3:c.839C= | NP_612422.2:p.Thr280= |
| ENST00000370646.8:c.839C= | ENSP00000359680.4:p.Thr280= |
| ENST00000370647.8:c.350C= | ENSP00000359681.4:p.Thr117= |
| ENST00000370649.3:c.345+9524C= | ENSP00000359683.3:n.345+9524C= |