Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151615621C>G , CM000668.2:g.151615621C>G | GRCh38 |
| NC_000006.11:g.151936756C>G , CM000668.1:g.151936756C>G | GRCh37 |
| NC_000006.10:g.151978449C>G | NCBI36 |
| NG_021198.1:g.126582C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.1889C>G MANE Select | ENSP00000239374.6:p.Thr630Ser | |
| ENST00000239374.7:c.1889C>G | ENSP00000239374.6:p.Thr630Ser | |
| NM_025059.3:c.1889C>G | NP_079335.2:p.Thr630Ser | |
| XM_011536147.1:c.1907C>G | XP_011534449.1:p.Thr636Ser | |
| XM_011536148.1:c.1706C>G | XP_011534450.1:p.Thr569Ser | |
| XM_011536147.2:c.1907C>G | XP_011534449.1:p.Thr636Ser | |
| XM_011536148.2:c.1706C>G | XP_011534450.1:p.Thr569Ser | |
| XR_001743865.1:n.129+1100G>C | ||
| NM_025059.4:c.1889C>G MANE Select | NP_079335.2:p.Thr630Ser |