Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38675843A>T , CM000685.2:g.38675843A>T | GRCh38 |
| NC_000023.10:g.38535097A>T , CM000685.1:g.38535097A>T | GRCh37 |
| NC_000023.9:g.38420041A>T | NCBI36 |
| NG_009160.1:g.119367A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378482.7:c.580A>T MANE Select | ENSP00000367743.2:p.Thr194Ser | |
| ENST00000286824.6:c.631A>T | ENSP00000286824.6:p.Thr211Ser | |
| ENST00000378482.6:c.580A>T | ENSP00000367743.2:p.Thr194Ser | |
| ENST00000419600.3:n.524A>T | ||
| ENST00000465127.1:c.670A>T | ENSP00000417050.1:p.Thr224Ser | |
| ENST00000471410.5:c.*606A>T | ENSP00000419290.1:n.*606A>T | |
| ENST00000475216.5:c.*573A>T | ENSP00000418586.1:n.*573A>T | |
| NM_004615.3:c.580A>T | NP_004606.2:p.Thr194Ser | |
| NM_004615.4:c.580A>T MANE Select | NP_004606.2:p.Thr194Ser |