Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400596C= , CM000670.2:g.18400596C= | GRCh38 |
| NC_000008.10:g.18258106C= , CM000670.1:g.18258106C= | GRCh37 |
| NC_000008.9:g.18302386C= | NCBI36 |
| NG_012246.1:g.14352C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.593C= MANE Select | ENSP00000286479.3:p.Thr198= | |
| ENST00000286479.3:c.593C= | ENSP00000286479.3:p.Thr198= | |
| ENST00000520116.1:c.203C= | ENSP00000428416.1:p.Thr68= | |
| NM_000015.2:c.593C= | NP_000006.2:p.Thr198= | |
| XM_011544358.1:c.593C= | XP_011542660.1:p.Thr198= | |
| XM_017012938.1:c.593C= | XP_016868427.1:p.Thr198= | |
| NM_000015.3:c.593C= MANE Select | NP_000006.2:p.Thr198= |