Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173583A>T , CM000678.2:g.173583A>T | GRCh38 |
| NC_000016.9:g.223582A>T , CM000678.1:g.223582A>T | GRCh37 |
| NC_000016.8:g.163582A>T | NCBI36 |
| NG_000006.1:g.34446A>T | |
| NG_059186.1:g.1933A>T | |
| NG_059271.1:g.5737A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.412A>T MANE Select | ENSP00000251595.6:p.Thr138Ser | |
| ENST00000251595.10:c.412A>T | ENSP00000251595.6:p.Thr138Ser | |
| ENST00000397806.1:c.316A>T | ENSP00000380908.1:p.Thr106Ser | |
| ENST00000482565.1:n.548A>T | ||
| NM_000517.4:c.412A>T | NP_000508.1:p.Thr138Ser | |
| NM_000517.6:c.412A>T MANE Select | NP_000508.1:p.Thr138Ser |