Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454418T>G , CM000679.2:g.7454418T>G | GRCh38 |
| NC_000017.10:g.7357737T>G , CM000679.1:g.7357737T>G | GRCh37 |
| NC_000017.9:g.7298461T>G | NCBI36 |
| NG_008026.1:g.14332T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.942T>G MANE Select | ENSP00000304290.2:p.Phe314Leu | |
| ENST00000306071.6:c.942T>G | ENSP00000304290.2:p.Phe314Leu | |
| ENST00000536404.6:c.726T>G | ENSP00000439209.2:p.Phe242Leu | |
| ENST00000570557.5:c.605T>G | ||
| ENST00000573209.1:n.1886T>G | ||
| ENST00000576360.1:c.605-26T>G | ENSP00000459092.1:n.605-26T>G | |
| NM_000747.2:c.942T>G | NP_000738.2:p.Phe314Leu | |
| NM_000747.3:c.942T>G MANE Select | NP_000738.2:p.Phe314Leu |