Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.64162974A>T , CM000677.2:g.64162974A>T | GRCh38 |
| NC_000015.9:g.64455173A>T , CM000677.1:g.64455173A>T | GRCh37 |
| NC_000015.8:g.62242226A>T | NCBI36 |
| NG_012979.1:g.5182T>A , LRG_10:g.5182T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300026.4:c.13T>A MANE Select | ENSP00000300026.4:p.Ser5Thr | |
| ENST00000561048.2:n.46T>A | ||
| ENST00000680158.1:c.13T>A | ENSP00000504873.1:p.Ser5Thr | |
| ENST00000681397.1:c.13T>A | ENSP00000506584.1:p.Ser5Thr | |
| ENST00000681658.1:c.13T>A | ENSP00000505431.1:p.Ser5Thr | |
| ENST00000300026.3:c.13T>A | ENSP00000300026.3:p.Ser5Thr | |
| ENST00000558492.1:n.33T>A | ||
| ENST00000561048.1:n.48T>A | ||
| NM_000942.4:c.13T>A , LRG_10t1:c.13T>A | NP_000933.1:p.Ser5Thr | |
| NM_000942.5:c.13T>A MANE Select | NP_000933.1:p.Ser5Thr |