Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24205027G>C , CM000668.2:g.24205027G>C | GRCh38 |
| NC_000006.11:g.24205255G>C , CM000668.1:g.24205255G>C | GRCh37 |
| NC_000006.10:g.24313234G>C | NCBI36 |
| NG_012829.1:g.158026C>G | |
| NG_012829.2:g.183266C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.998C>G MANE Select | ENSP00000367715.3:p.Thr333Ser | |
| ENST00000378450.6:c.257C>G | ENSP00000367711.3:p.Thr86Ser | |
| ENST00000378454.7:c.998C>G | ENSP00000367715.3:p.Thr333Ser | |
| NM_001195610.1:c.998C>G | NP_001182539.1:p.Thr333Ser | |
| NM_016356.4:c.998C>G | NP_057440.2:p.Thr333Ser | |
| NM_016356.5:c.998C>G MANE Select | NP_057440.2:p.Thr333Ser | |
| NM_001195610.2:c.998C>G | NP_001182539.1:p.Thr333Ser |