gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00015861 (NFE)
Genomes Max Group AF
0.00005847 (NFE)
Exomes Max Group AF
0.00016195 (NFE)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.169477137G>A , CM000666.2:g.169477137G>A | GRCh38 |
| NC_000004.11:g.170398288G>A , CM000666.1:g.170398288G>A | GRCh37 |
| NC_000004.10:g.170634863G>A | NCBI36 |
| NG_027982.1:g.140491C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685111.1:c.2253C>T | ENSP00000508844.1:p.Phe751= | |
| ENST00000685677.1:n.1719C>T | ||
| ENST00000686697.1:c.2115C>T | ENSP00000508689.1:p.Phe705= | |
| ENST00000687054.1:n.2915C>T | ||
| ENST00000687528.1:c.*1156C>T | ENSP00000510228.1:n.*1156C>T | |
| ENST00000687643.1:c.2364C>T | ENSP00000509309.1:p.Phe788= | |
| ENST00000688934.1:c.444C>T | ENSP00000510760.1:p.Phe148= | |
| ENST00000690540.1:n.1871C>T | ||
| ENST00000507142.6:c.2421C>T MANE Select | ENSP00000424757.2:p.Phe807= | |
| ENST00000638824.1:n.549C>T | ||
| ENST00000439128.6:c.2337C>T | ENSP00000408020.2:p.Phe779= | |
| ENST00000507142.5:c.2421C>T | ENSP00000424757.1:p.Phe807= | |
| ENST00000510533.5:c.2205C>T | ENSP00000427653.1:p.Phe735= | |
| ENST00000511633.5:c.2289C>T | ENSP00000423332.1:p.Phe763= | |
| ENST00000512193.5:c.2130C>T | ENSP00000424938.1:p.Phe710= | |
| NM_001199397.1:c.2421C>T | NP_001186326.1:p.Phe807= | |
| NM_001199398.1:c.2289C>T | NP_001186327.1:p.Phe763= | |
| NM_001199399.1:c.2130C>T | NP_001186328.1:p.Phe710= | |
| NM_001199400.1:c.2205C>T | NP_001186329.1:p.Phe735= | |
| NM_012224.2:c.2337C>T | NP_036356.1:p.Phe779= | |
| XM_006714228.1:c.2421C>T | XP_006714291.1:p.Phe807= | |
| XM_011532003.1:c.2337C>T | XP_011530305.1:p.Phe779= | |
| XM_011532004.1:c.2205C>T | XP_011530306.1:p.Phe735= | |
| XM_017008249.1:c.1800C>T | XP_016863738.1:p.Phe600= | |
| XM_017008251.1:c.1716C>T | XP_016863740.1:p.Phe572= | |
| XM_017008252.2:c.1716C>T | XP_016863741.1:p.Phe572= | |
| XM_017008253.1:c.1269C>T | XP_016863742.1:p.Phe423= | |
| XM_017008254.1:c.1065C>T | XP_016863743.1:p.Phe355= | |
| XM_024454065.1:c.1800C>T | XP_024309833.1:p.Phe600= | |
| XR_001741233.1:n.2719+2266C>T | ||
| XR_001741234.2:n.3697C>T | ||
| NM_001199397.3:c.2421C>T MANE Select | NP_001186326.1:p.Phe807= | |
| NM_001199398.2:c.2289C>T | NP_001186327.1:p.Phe763= | |
| NM_001199399.2:c.2130C>T | NP_001186328.1:p.Phe710= | |
| NM_001199400.2:c.2205C>T | NP_001186329.1:p.Phe735= | |
| NM_001374418.1:c.2421C>T | NP_001361347.1:p.Phe807= | |
| NM_001374419.1:c.2337C>T | NP_001361348.1:p.Phe779= | |
| NM_001374420.1:c.2286C>T | NP_001361349.1:p.Phe762= | |
| NM_001374421.1:c.2115C>T | NP_001361350.1:p.Phe705= | |
| NM_012224.3:c.2337C>T | NP_036356.1:p.Phe779= | |
| NR_164630.1:n.2883C>T | ||
| NM_001199398.3:c.2289C>T | NP_001186327.1:p.Phe763= | |
| NM_001199399.3:c.2130C>T | NP_001186328.1:p.Phe710= | |
| NM_001199400.3:c.2205C>T | NP_001186329.1:p.Phe735= | |
| NM_012224.4:c.2337C>T | NP_036356.1:p.Phe779= |