Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44251305T= , CM000679.2:g.44251305T= | GRCh38 |
| NC_000017.10:g.42328673T= , CM000679.1:g.42328673T= | GRCh37 |
| NC_000017.9:g.39684199T= | NCBI36 |
| NG_007498.1:g.21830A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000342.4:c.2509A= MANE Select | NP_000333.1:p.Thr837= |
| ENST00000262418.12:c.2509A= MANE Select | ENSP00000262418.6:p.Thr837= |
| NM_000342.3:c.2509A= | NP_000333.1:p.Thr837= |
| ENST00000262418.10:c.2509A= | ENSP00000262418.6:p.Thr837= |
| ENST00000399246.3:c.1411A= | ENSP00000382190.3:p.Thr471= |
| XM_005257593.3:c.2314A= | XP_005257650.1:p.Thr772= |
| XM_005257593.5:c.2314A= | XP_005257650.1:p.Thr772= |
| XM_011525129.1:c.2419A= | XP_011523431.1:p.Thr807= |
| XM_011525129.2:c.2419A= | XP_011523431.1:p.Thr807= |