Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670449G= , CM000666.2:g.68670449G= | GRCh38 |
| NC_000004.11:g.69536167G= , CM000666.1:g.69536167G= | GRCh37 |
| NC_000004.10:g.69218762G= | NCBI36 |
| NG_052676.1:g.5328C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.170C= MANE Select | ENSP00000341045.5:p.Thr57= | |
| ENST00000338206.5:c.170C= | ENSP00000341045.5:p.Thr57= | |
| ENST00000616841.4:c.170C= | ENSP00000482004.1:p.Thr57= | |
| NM_001076.3:c.170C= | NP_001067.2:p.Thr57= | |
| NM_001076.4:c.170C= MANE Select | NP_001067.2:p.Thr57= |