Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.59269118G>T , CM000680.2:g.59269118G>T | GRCh38 |
| NC_000018.9:g.56936350G>T , CM000680.1:g.56936350G>T | GRCh37 |
| NC_000018.8:g.55087330G>T | NCBI36 |
| NG_013031.1:g.9276C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334889.4:c.927C>A MANE Select | ENSP00000334813.3:p.Phe309Leu | |
| ENST00000256852.7:c.*358C>A | ENSP00000256852.7:n.*358C>A | |
| ENST00000334889.3:c.927C>A | ENSP00000334813.3:p.Phe309Leu | |
| NM_013435.2:c.927C>A | NP_038463.2:p.Phe309Leu | |
| NM_013435.3:c.927C>A MANE Select | NP_038463.2:p.Phe309Leu |