Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15889447G>C , CM000681.2:g.15889447G>C | GRCh38 |
| NC_000019.9:g.16000257G>C , CM000681.1:g.16000257G>C | GRCh37 |
| NC_000019.8:g.15861257G>C | NCBI36 |
| NG_007971.2:g.13628C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.894C>G MANE Select | ENSP00000221700.3:p.Phe298Leu | |
| ENST00000011989.11:c.894C>G | ENSP00000011989.8:p.Phe298Leu | |
| ENST00000221700.10:c.894C>G | ENSP00000221700.3:p.Phe298Leu | |
| ENST00000392846.7:n.837C>G | ||
| ENST00000587671.2:c.*479C>G | ENSP00000467443.2:n.*479C>G | |
| NM_001082.4:c.894C>G | NP_001073.3:p.Phe298Leu | |
| NM_001082.5:c.894C>G MANE Select | NP_001073.3:p.Phe298Leu |