Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658696A>T , CM000682.2:g.10658696A>T | GRCh38 |
| NC_000020.10:g.10639344A>T , CM000682.1:g.10639344A>T | GRCh37 |
| NC_000020.9:g.10587344A>T | NCBI36 |
| NG_007496.1:g.20351T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.466T>A MANE Select | ENSP00000254958.4:p.Ser156Thr | |
| ENST00000254958.9:c.466T>A | ENSP00000254958.4:p.Ser156Thr | |
| ENST00000423891.6:n.332T>A | ||
| NM_000214.2:c.466T>A | NP_000205.1:p.Ser156Thr | |
| NM_000214.3:c.466T>A MANE Select | NP_000205.1:p.Ser156Thr |