Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46003478T>G , CM000683.2:g.46003478T>G | GRCh38 |
| NC_000021.8:g.47423392T>G , CM000683.1:g.47423392T>G | GRCh37 |
| NC_000021.7:g.46247820T>G | NCBI36 |
| NG_008674.1:g.26730T>G , LRG_475:g.26730T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000463060.6:n.951T>G | ||
| ENST00000612273.2:c.678T>G | ||
| ENST00000682634.1:c.678T>G | ||
| ENST00000361866.8:c.2552T>G MANE Select | ENSP00000355180.3:p.Phe851Cys | |
| ENST00000361866.7:c.2552T>G | ENSP00000355180.3:p.Phe851Cys | |
| ENST00000486023.1:n.340T>G | ||
| ENST00000498614.5:n.786T>G | ||
| ENST00000612273.1:c.2546T>G | ENSP00000483630.1:p.Phe849Cys | |
| NM_001848.2:c.2552T>G , LRG_475t1:c.2552T>G | NP_001839.2:p.Phe851Cys | |
| NM_001848.3:c.2552T>G MANE Select | NP_001839.2:p.Phe851Cys |