Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107696017A>T , CM000669.2:g.107696017A>T | GRCh38 |
| NC_000007.13:g.107336462A>T , CM000669.1:g.107336462A>T | GRCh37 |
| NC_000007.12:g.107123698A>T | NCBI36 |
| NG_008489.1:g.40383A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1522A>T MANE Select | ENSP00000494017.1:p.Thr508Ser | |
| ENST00000644846.1:c.233A>T | ||
| ENST00000265715.7:c.1522A>T | ENSP00000265715.3:p.Thr508Ser | |
| ENST00000477350.5:n.369A>T | ||
| ENST00000480841.5:n.371A>T | ||
| ENST00000497446.5:n.537A>T | ||
| NM_000441.1:c.1522A>T | NP_000432.1:p.Thr508Ser | |
| XM_005250425.1:c.1522A>T | XP_005250482.1:p.Thr508Ser | |
| XM_005250425.2:c.1522A>T | XP_005250482.1:p.Thr508Ser | |
| XM_017012318.1:c.1444A>T | XP_016867807.1:p.Thr482Ser | |
| NM_000441.2:c.1522A>T MANE Select | NP_000432.1:p.Thr508Ser |