Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119422277C= , CM000663.2:g.119422277C= | GRCh38 |
| NC_000001.10:g.119964900C= , CM000663.1:g.119964900C= | GRCh37 |
| NC_000001.9:g.119766423C= | NCBI36 |
| NG_013349.1:g.12347C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000198.4:c.776C= MANE Select | NP_000189.1:p.Thr259= |
| ENST00000369416.4:c.776C= MANE Select | ENSP00000358424.3:p.Thr259= |
| NM_000198.3:c.776C= | NP_000189.1:p.Thr259= |
| NM_001166120.1:c.776C= | NP_001159592.1:p.Thr259= |
| NM_001166120.2:c.776C= | NP_001159592.1:p.Thr259= |
| ENST00000369416.3:c.776C= | ENSP00000358424.3:p.Thr259= |
| ENST00000543831.5:c.776C= | ENSP00000445122.1:p.Thr259= |