Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506793A= , CM000672.2:g.122506793A= | GRCh38 |
| NC_000010.10:g.124266309A= , CM000672.1:g.124266309A= | GRCh37 |
| NC_000010.9:g.124256299A= | NCBI36 |
| NG_011554.1:g.50269A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.880A= MANE Select | ENSP00000357980.3:p.Thr294= | |
| ENST00000648167.1:c.562A= | ENSP00000498033.1:p.Thr188= | |
| ENST00000368984.7:c.880A= | ENSP00000357980.3:p.Thr294= | |
| ENST00000420892.1:c.103A= | ENSP00000412676.1:p.Thr35= | |
| NM_002775.4:c.880A= | NP_002766.1:p.Thr294= | |
| NM_002775.5:c.880A= MANE Select | NP_002766.1:p.Thr294= |