Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.98186926C>G , CM000669.2:g.98186926C>G | GRCh38 |
| NC_000007.13:g.97816238C>G , CM000669.1:g.97816238C>G | GRCh37 |
| NC_000007.12:g.97654174C>G | NCBI36 |
| NG_013375.1:g.85042C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297293.6:c.926C>G MANE Select | ENSP00000297293.5:p.Thr309Ser | |
| ENST00000297293.5:c.926C>G | ENSP00000297293.5:p.Thr309Ser | |
| NM_014916.3:c.926C>G | NP_055731.2:p.Thr309Ser | |
| XM_011515981.1:c.920C>G | XP_011514283.1:p.Thr307Ser | |
| XM_011515981.3:c.920C>G | XP_011514283.1:p.Thr307Ser | |
| NM_014916.4:c.926C>G MANE Select | NP_055731.2:p.Thr309Ser |