Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945946T= , CM000665.2:g.138945946T= | GRCh38 |
| NC_000003.11:g.138664788T= , CM000665.1:g.138664788T= | GRCh37 |
| NC_000003.10:g.140147478T= | NCBI36 |
| NG_012454.1:g.6195A= | |
| NG_029796.1:g.3713T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.777A= MANE Select | ENSP00000497217.1:p.Thr259= | |
| ENST00000330315.3:c.777A= | ENSP00000333188.3:p.Thr259= | |
| NM_023067.3:c.777A= | NP_075555.1:p.Thr259= | |
| NM_023067.4:c.777A= MANE Select | NP_075555.1:p.Thr259= |