Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154758T>A , CM000681.2:g.55154758T>A | GRCh38 |
| NC_000019.9:g.55666126T>A , CM000681.1:g.55666126T>A | GRCh37 |
| NC_000019.8:g.60357938T>A | NCBI36 |
| NG_007866.2:g.7975A>T , LRG_432:g.7975A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.355A>T MANE Select | ENSP00000341838.5:p.Thr119Ser | |
| ENST00000665070.1:c.355A>T | ENSP00000499482.1:p.Thr119Ser | |
| ENST00000344887.9:c.355A>T | ENSP00000341838.5:p.Thr119Ser | |
| ENST00000585806.5:n.354A>T | ||
| ENST00000586669.5:n.363A>T | ||
| ENST00000587176.5:n.539A>T | ||
| ENST00000587871.1:c.974A>T | ||
| ENST00000588882.1:c.280A>T | ENSP00000466729.1:p.Thr94Ser | |
| ENST00000590463.1:n.527A>T | ||
| NM_000363.4:c.355A>T , LRG_432t1:c.355A>T | NP_000354.4:p.Thr119Ser | |
| NM_000363.5:c.355A>T MANE Select | NP_000354.4:p.Thr119Ser |