Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47582359T>G , CM000673.2:g.47582359T>G | GRCh38 |
| NC_000011.9:g.47603911T>G , CM000673.1:g.47603911T>G | GRCh37 |
| NC_000011.8:g.47560487T>G | NCBI36 |
| NG_011946.1:g.8350T>G | |
| NG_011946.2:g.8350T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263774.9:c.518T>G MANE Select | ENSP00000263774.4:p.Met173Arg | |
| ENST00000531351.2:n.1713T>G | ||
| ENST00000677462.1:n.2992T>G | ||
| ENST00000678975.1:n.2775T>G | ||
| ENST00000263774.8:c.518T>G | ENSP00000263774.4:p.Met173Arg | |
| ENST00000524568.1:n.621T>G | ||
| ENST00000525212.1:n.173T>G | ||
| ENST00000525378.5:n.456T>G | ||
| ENST00000527178.1:n.118T>G | ||
| ENST00000533507.5:n.1412T>G | ||
| NM_004551.2:c.518T>G | NP_004542.1:p.Met173Arg | |
| NM_004551.3:c.518T>G MANE Select | NP_004542.1:p.Met173Arg |