Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3082726C= , CM000682.2:g.3082726C= | GRCh38 |
| NC_000020.10:g.3063372C= , CM000682.1:g.3063372C= | GRCh37 |
| NC_000020.9:g.3011372C= | NCBI36 |
| NG_008663.1:g.6999G= , LRG_715:g.6999G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.399G= MANE Select | ENSP00000369647.3:p.Thr133= | |
| NM_000490.4:c.399G= , LRG_715t1:c.399G= | NP_000481.2:p.Thr133= | |
| XM_011529267.1:c.399G= | XP_011527569.1:p.Thr133= | |
| XM_011529267.2:c.399G= | XP_011527569.1:p.Thr133= | |
| NM_000490.5:c.399G= MANE Select | NP_000481.2:p.Thr133= |