Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508776C>G , CM000685.2:g.83508776C>G | GRCh38 |
| NC_000023.10:g.82763784C>G , CM000685.1:g.82763784C>G | GRCh37 |
| NC_000023.9:g.82650440C>G | NCBI36 |
| NG_009936.2:g.5516C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644024.2:c.452C>G MANE Select | ENSP00000495996.1:p.Thr151Ser | |
| ENST00000373200.4:c.452C>G | ENSP00000362296.2:p.Thr151Ser | |
| NM_000307.4:c.452C>G | NP_000298.3:p.Thr151Ser | |
| NM_000307.5:c.452C>G MANE Select | NP_000298.3:p.Thr151Ser |