Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47375237G= , CM000664.2:g.47375237G= | GRCh38 |
| NC_000002.11:g.47602376G= , CM000664.1:g.47602376G= | GRCh37 |
| NC_000002.10:g.47455880G= | NCBI36 |
| NG_012352.2:g.35075G= , LRG_215:g.35075G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263735.9:c.429G= MANE Select | ENSP00000263735.4:p.Trp143= | |
| ENST00000263735.8:c.429G= | ENSP00000263735.4:p.Trp143= | |
| ENST00000405271.5:c.513G= | ENSP00000385476.1:p.Trp171= | |
| ENST00000456133.5:c.513G= | ENSP00000410675.1:p.Trp171= | |
| ENST00000474691.1:n.697G= | ||
| ENST00000490733.1:n.278G= | ||
| NM_002354.2:c.429G= , LRG_215t1:c.429G= | NP_002345.2:p.Trp143= | |
| NM_002354.3:c.429G= MANE Select | NP_002345.2:p.Trp143= |