Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52519756A>T , CM000674.2:g.52519756A>T | GRCh38 |
| NC_000012.11:g.52913540A>T , CM000674.1:g.52913540A>T | GRCh37 |
| NC_000012.10:g.51199807A>T | NCBI36 |
| NG_008297.1:g.5704T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000424.4:c.541T>A MANE Select | NP_000415.2:p.Ser181Thr |
| ENST00000252242.9:c.541T>A MANE Select | ENSP00000252242.4:p.Ser181Thr |
| NM_000424.3:c.541T>A | NP_000415.2:p.Ser181Thr |
| ENST00000252242.8:c.541T>A | ENSP00000252242.4:p.Ser181Thr |
| ENST00000549420.1:c.211T>A | ENSP00000447209.1:p.Ser71Thr |
| ENST00000551275.1:c.436T>A | ENSP00000448041.1:p.Ser146Thr |
| ENST00000552629.5:n.639T>A |