Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99845685T>C , CM000672.2:g.99845685T>C | GRCh38 |
| NC_000010.10:g.101605442T>C , CM000672.1:g.101605442T>C | GRCh37 |
| NC_000010.9:g.101595432T>C | NCBI36 |
| NG_011798.1:g.67980T>C | |
| NG_011798.2:g.68088T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.4049T>C MANE Select | ENSP00000497274.1:p.Ile1350Thr | |
| ENST00000649459.1:n.397T>C | ||
| ENST00000370449.8:c.4049T>C | ENSP00000359478.4:p.Ile1350Thr | |
| NM_000392.4:c.4049T>C | NP_000383.1:p.Ile1350Thr | |
| XM_006717630.2:c.3353T>C | XP_006717693.1:p.Ile1118Thr | |
| XR_945604.1:n.4179T>C | ||
| XR_945605.1:n.4113T>C | ||
| NM_000392.5:c.4049T>C MANE Select | NP_000383.2:p.Ile1350Thr | |
| XM_006717630.3:c.3353T>C | XP_006717693.1:p.Ile1118Thr | |
| XR_945604.3:n.4233T>C | ||
| XR_945605.3:n.4165T>C |