Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872534C>G , CM000673.2:g.124872534C>G | GRCh38 |
| NC_000011.9:g.124742430C>G , CM000673.1:g.124742430C>G | GRCh37 |
| NC_000011.8:g.124247640C>G | NCBI36 |
| NG_016214.1:g.12126C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1312C>G MANE Select | ENSP00000380903.1:p.Leu438Val | |
| ENST00000397801.5:c.1312C>G | ENSP00000380903.1:p.Leu438Val | |
| ENST00000538940.5:c.1246C>G | ENSP00000441797.1:p.Leu416Val | |
| NM_022370.3:c.1312C>G | NP_071765.2:p.Leu438Val | |
| XM_011542953.1:c.2284C>G | XP_011541255.1:p.Leu762Val | |
| XM_017018122.1:c.1246C>G | XP_016873611.1:p.Leu416Val | |
| NM_022370.4:c.1312C>G MANE Select | NP_071765.2:p.Leu438Val |