Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99845657T>A , CM000672.2:g.99845657T>A | GRCh38 |
| NC_000010.10:g.101605414T>A , CM000672.1:g.101605414T>A | GRCh37 |
| NC_000010.9:g.101595404T>A | NCBI36 |
| NG_011798.1:g.67952T>A | |
| NG_011798.2:g.68060T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.4021T>A MANE Select | ENSP00000497274.1:p.Ser1341Thr | |
| ENST00000649459.1:n.369T>A | ||
| ENST00000370449.8:c.4021T>A | ENSP00000359478.4:p.Ser1341Thr | |
| NM_000392.4:c.4021T>A | NP_000383.1:p.Ser1341Thr | |
| XM_006717630.2:c.3325T>A | XP_006717693.1:p.Ser1109Thr | |
| XR_945604.1:n.4177-26T>A | ||
| XR_945605.1:n.4085T>A | ||
| NM_000392.5:c.4021T>A MANE Select | NP_000383.2:p.Ser1341Thr | |
| XM_006717630.3:c.3325T>A | XP_006717693.1:p.Ser1109Thr | |
| XR_945604.3:n.4231-26T>A | ||
| XR_945605.3:n.4137T>A |