COSMIC:
COSM3753697 (not active)
COSM3753698 (not active)
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.73699092 (EAS)
Genomes Max Group AF
0.73173065 (EAS)
Exomes Max Group AF
0.73556097 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.42219343G>A , CM000675.2:g.42219343G>A | GRCh38 |
| NC_000013.10:g.42793479G>A , CM000675.1:g.42793479G>A | GRCh37 |
| NC_000013.9:g.41691479G>A | NCBI36 |
| NG_029191.2:g.184308G>A | |
| NG_029191.3:g.184308G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337343.9:c.3327G>A MANE Select | ENSP00000337572.4:p.Glu1109= | |
| ENST00000261491.9:c.3327G>A | ENSP00000261491.4:p.Glu1109= | |
| ENST00000337343.8:c.3327G>A | ENSP00000337572.4:p.Glu1109= | |
| ENST00000379274.6:c.3327G>A | ENSP00000368576.3:p.Glu1109= | |
| ENST00000498255.6:n.3753G>A | ||
| ENST00000536612.3:c.2919G>A | ENSP00000445114.2:p.Glu973= | |
| ENST00000626247.2:c.*2416G>A | ENSP00000486329.1:n.*2416G>A | |
| ENST00000627777.2:c.2919G>A | ENSP00000486838.1:p.Glu973= | |
| ENST00000628433.2:c.2919G>A | ENSP00000485809.1:p.Glu973= | |
| NM_001204504.2:c.3327G>A | NP_001191433.1:p.Glu1109= | |
| NM_001204505.2:c.2919G>A | NP_001191434.1:p.Glu973= | |
| NM_001204506.2:c.2919G>A | NP_001191435.1:p.Glu973= | |
| NM_001297429.1:c.2592G>A | NP_001284358.1:p.Glu864= | |
| NM_152910.5:c.3327G>A | NP_690874.2:p.Glu1109= | |
| NM_178009.4:c.3327G>A | NP_821077.1:p.Glu1109= | |
| NR_123714.1:n.3051G>A | ||
| NR_123715.1:n.3859G>A | ||
| NM_001204505.3:c.2919G>A | NP_001191434.1:p.Glu973= | |
| NM_001204506.3:c.2919G>A | NP_001191435.1:p.Glu973= | |
| NM_001297429.2:c.2592G>A | NP_001284358.1:p.Glu864= | |
| NM_152910.6:c.3327G>A | NP_690874.2:p.Glu1109= | |
| NM_178009.5:c.3327G>A MANE Select | NP_821077.1:p.Glu1109= | |
| NR_123714.2:n.3035G>A | ||
| NR_123715.2:n.3843G>A | ||
| NM_001204504.3:c.3327G>A | NP_001191433.1:p.Glu1109= |