Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73442356G= , CM000666.2:g.73442356G= | GRCh38 |
| NC_000004.11:g.74308073G= , CM000666.1:g.74308073G= | GRCh37 |
| NC_000004.10:g.74526937G= | NCBI36 |
| NG_023028.1:g.11141G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395792.7:c.543G= MANE Select | ENSP00000379138.2:p.Trp181= | |
| ENST00000226359.2:c.543G= | ENSP00000226359.2:p.Trp181= | |
| ENST00000395792.6:c.543G= | ENSP00000379138.2:p.Trp181= | |
| NM_001134.2:c.543G= | NP_001125.1:p.Trp181= | |
| XM_011531704.1:c.540G= | XP_011530006.1:p.Trp180= | |
| NM_001354717.1:c.69G= | NP_001341646.1:p.Trp23= | |
| NM_001134.3:c.543G= MANE Select | NP_001125.1:p.Trp181= | |
| NM_001354717.2:c.69G= | NP_001341646.2:p.Trp23= |