Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7933910A>C , CM000681.2:g.7933910A>C | GRCh38 |
| NC_000019.9:g.7998795A>C , CM000681.1:g.7998795A>C | GRCh37 |
| NC_000019.8:g.7904795A>C | NCBI36 |
| NG_051180.1:g.14914T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270538.8:c.637T>G MANE Select | ENSP00000270538.2:p.Phe213Val | |
| ENST00000270538.7:c.637T>G | ENSP00000270538.2:p.Phe213Val | |
| ENST00000595831.5:c.624T>G | ||
| ENST00000595876.5:c.*325T>G | ENSP00000471596.1:n.*325T>G | |
| ENST00000597926.1:c.541T>G | ENSP00000469389.1:p.Phe181Val | |
| ENST00000598675.1:n.43T>G | ||
| ENST00000600748.5:n.622T>G | ||
| NM_006351.3:c.637T>G | NP_006342.2:p.Phe213Val | |
| NM_006351.4:c.637T>G MANE Select | NP_006342.2:p.Phe213Val |