Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562854T>G , CM000682.2:g.57562854T>G | GRCh38 |
| NC_000020.10:g.56137910T>G , CM000682.1:g.56137910T>G | GRCh37 |
| NC_000020.9:g.55571316T>G | NCBI36 |
| NG_008205.1:g.6774T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.565T>G MANE Select | ENSP00000319814.4:p.Phe189Val | |
| ENST00000319441.5:c.565T>G | ENSP00000319814.4:p.Phe189Val | |
| ENST00000467047.1:n.1775T>G | ||
| ENST00000470051.1:n.21T>G | ||
| ENST00000498194.1:n.507T>G | ||
| NM_002591.3:c.565T>G | NP_002582.3:p.Phe189Val | |
| XM_011528839.1:c.169T>G | XP_011527141.1:p.Phe57Val | |
| XM_024451888.1:c.169T>G | XP_024307656.1:p.Phe57Val | |
| NM_002591.4:c.565T>G MANE Select | NP_002582.3:p.Phe189Val |