MyVariant.info:
GRCh38
chr16:g.10902076G>A
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.04671473 (AFR)
Genomes Max Group AF
0.04546272 (AFR)
Exomes Max Group AF
0.04707006 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.10902076G>A , CM000678.2:g.10902076G>A | GRCh38 |
| NG_009628.1:g.29879G>A , LRG_49:g.29879G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695879.1:n.545G>A | ||
| ENST00000324288.14:c.520G>A MANE Select | ENSP00000316328.8:p.Gly174Arg | |
| ENST00000637439.1:c.754G>A | ENSP00000489907.1:p.Gly252Arg | |
| ENST00000324288.12:c.520G>A | ENSP00000316328.8:p.Gly174Arg | |
| ENST00000381835.9:c.481+518G>A | ENSP00000371257.5:n.481+518G>A | |
| ENST00000537380.1:n.520G>A | ||
| ENST00000570546.5:n.641G>A | ||
| ENST00000571186.5:c.*241G>A | ENSP00000459829.1:n.*241G>A | |
| ENST00000573309.5:n.599+518G>A | ||
| ENST00000576601.1:c.448G>A | ENSP00000459608.1:p.Gly150Arg | |
| ENST00000611587.4:c.484+518G>A | ENSP00000483487.1:n.484+518G>A | |
| ENST00000618207.4:c.520G>A | ENSP00000484761.1:p.Gly174Arg | |
| ENST00000618327.4:c.523G>A | ENSP00000485010.1:p.Gly175Arg | |
| NM_000246.3:c.520G>A , LRG_49t1:c.520G>A | NP_000237.2:p.Gly174Arg | |
| NM_001286402.1:c.523G>A | NP_001273331.1:p.Gly175Arg | |
| NM_001286403.1:c.481+518G>A | NP_001273332.1:n.481+518G>A | |
| NR_104444.1:n.653G>A | ||
| XM_006720880.2:c.817G>A | XP_006720943.2:p.Gly273Arg | |
| XM_011522484.1:c.817G>A | XP_011520786.1:p.Gly273Arg | |
| XM_011522485.1:c.817G>A | XP_011520787.1:p.Gly273Arg | |
| XM_011522486.1:c.817G>A | XP_011520788.1:p.Gly273Arg | |
| XM_011522487.1:c.679+518G>A | XP_011520789.1:n.679+518G>A | |
| XM_011522488.1:c.568G>A | XP_011520790.1:p.Gly190Arg | |
| XM_011522489.1:c.676+518G>A | XP_011520791.1:n.676+518G>A | |
| XM_011522490.1:c.565G>A | XP_011520792.1:p.Gly189Arg | |
| XM_011522491.1:c.817G>A | XP_011520793.1:p.Gly273Arg | |
| XM_011522492.1:c.523G>A | XP_011520794.1:p.Gly175Arg | |
| XM_011522493.1:c.520G>A | XP_011520795.1:p.Gly174Arg | |
| XM_011522494.1:c.451G>A | XP_011520796.1:p.Gly151Arg | |
| XM_011522495.1:c.484+518G>A | XP_011520797.1:n.484+518G>A | |
| XM_011522496.1:c.481+518G>A | XP_011520798.1:n.481+518G>A | |
| XR_932841.1:n.832G>A | ||
| XR_932842.1:n.832G>A | ||
| XR_932843.1:n.832G>A | ||
| XR_932846.1:n.832G>A | ||
| XR_932847.1:n.832G>A | ||
| XR_932848.1:n.631+518G>A | ||
| XM_006720880.3:c.817G>A | XP_006720943.2:p.Gly273Arg | |
| XM_011522484.3:c.817G>A | XP_011520786.1:p.Gly273Arg | |
| XM_011522485.2:c.817G>A | XP_011520787.1:p.Gly273Arg | |
| XM_011522486.2:c.817G>A | XP_011520788.1:p.Gly273Arg | |
| XM_011522487.2:c.679+518G>A | XP_011520789.1:n.679+518G>A | |
| XM_011522488.2:c.568G>A | XP_011520790.1:p.Gly190Arg | |
| XM_011522489.2:c.676+518G>A | XP_011520791.1:n.676+518G>A | |
| XM_011522490.2:c.565G>A | XP_011520792.1:p.Gly189Arg | |
| XM_011522491.2:c.817G>A | XP_011520793.1:p.Gly273Arg | |
| XM_011522492.2:c.523G>A | XP_011520794.1:p.Gly175Arg | |
| XM_011522493.2:c.520G>A | XP_011520795.1:p.Gly174Arg | |
| XM_011522494.2:c.451G>A | XP_011520796.1:p.Gly151Arg | |
| XM_011522495.2:c.484+518G>A | XP_011520797.1:n.484+518G>A | |
| XM_011522496.2:c.481+518G>A | XP_011520798.1:n.481+518G>A | |
| XM_024450280.1:c.763G>A | XP_024306048.1:p.Gly255Arg | |
| XM_024450281.1:c.724+518G>A | XP_024306049.1:n.724+518G>A | |
| XR_001751904.1:n.836G>A | ||
| XR_932841.3:n.834G>A | ||
| XR_932842.2:n.834G>A | ||
| XR_932846.3:n.836G>A | ||
| XR_932847.3:n.836G>A | ||
| NM_001286403.2:c.481+518G>A | NP_001273332.1:n.481+518G>A | |
| NR_104444.2:n.649G>A | ||
| NM_000246.4:c.520G>A MANE Select | NP_000237.2:p.Gly174Arg | |
| NM_001379330.1:c.484+518G>A | NP_001366259.1:n.484+518G>A | |
| NM_001379331.1:c.481+518G>A | NP_001366260.1:n.481+518G>A | |
| NM_001379332.1:c.523G>A | NP_001366261.1:p.Gly175Arg | |
| NM_001379333.1:c.520G>A | NP_001366262.1:p.Gly174Arg | |
| NM_001379334.1:c.451G>A | NP_001366263.1:p.Gly151Arg |