Linked Data
ClinVar Variation Id:
844951
dbSNP Id:
rs781223072
ExAC:
20:35559226 C / G
gnomAD v2:
20-35559226-C-G
gnomAD v3:
20-36930823-C-G
gnomAD v4:
20-36930823-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.36930823C>G , CM000682.2:g.36930823C>G | GRCh38 |
| NC_000020.10:g.35559226C>G , CM000682.1:g.35559226C>G | GRCh37 |
| NC_000020.9:g.34992640C>G | NCBI36 |
| NG_017059.1:g.26021G>C , LRG_281:g.26021G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644114.2:c.562G>C | ENSP00000494354.2:p.Glu188Gln | |
| ENST00000644250.2:c.562G>C | ENSP00000493810.2:p.Glu188Gln | |
| ENST00000644688.2:n.624G>C | ||
| ENST00000645444.2:c.562G>C | ENSP00000495381.2:p.Glu188Gln | |
| ENST00000682773.1:c.562G>C | ENSP00000507178.1:p.Glu188Gln | |
| ENST00000683720.1:c.562G>C | ENSP00000508219.1:p.Glu188Gln | |
| ENST00000683766.1:c.562G>C | ENSP00000506877.1:p.Glu188Gln | |
| ENST00000262878.5:c.562G>C | ENSP00000262878.5:p.Glu188Gln | |
| ENST00000642186.1:c.562G>C | ENSP00000494436.1:p.Glu188Gln | |
| ENST00000642246.1:c.*241G>C | ENSP00000494979.1:n.*241G>C | |
| ENST00000642616.1:c.*39G>C | ENSP00000494271.1:n.*39G>C | |
| ENST00000643078.1:c.*241G>C | ENSP00000496474.1:n.*241G>C | |
| ENST00000643161.1:n.125G>C | ||
| ENST00000643918.1:c.562G>C | ENSP00000493928.1:p.Glu188Gln | |
| ENST00000644114.1:c.488G>C | ||
| ENST00000644370.1:n.503G>C | ||
| ENST00000645033.1:c.562G>C | ENSP00000494520.1:p.Glu188Gln | |
| ENST00000645444.1:c.330G>C | ||
| ENST00000646066.1:c.562G>C | ENSP00000495432.1:p.Glu188Gln | |
| ENST00000646121.1:c.279G>C | ||
| ENST00000646673.2:c.562G>C MANE Select | ENSP00000493536.2:p.Glu188Gln | |
| ENST00000646866.1:c.*11G>C | ENSP00000495737.1:n.*11G>C | |
| ENST00000646869.1:c.562G>C | ENSP00000495667.1:p.Glu188Gln | |
| ENST00000646904.1:c.562G>C | ENSP00000494823.1:p.Glu188Gln | |
| ENST00000647095.1:n.633G>C | ||
| ENST00000647163.1:c.562G>C | ENSP00000494313.1:p.Glu188Gln | |
| ENST00000647459.1:n.589G>C | ||
| ENST00000262878.4:c.562G>C | ENSP00000262878.4:p.Glu188Gln | |
| NM_015474.3:c.562G>C , LRG_281t1:c.562G>C | NP_056289.2:p.Glu188Gln | |
| XM_005260384.2:c.562G>C | XP_005260441.1:p.Glu188Gln | |
| XM_011528761.1:c.562G>C | XP_011527063.1:p.Glu188Gln | |
| NM_001363729.1:c.562G>C | NP_001350658.1:p.Glu188Gln | |
| NM_001363733.1:c.562G>C | NP_001350662.1:p.Glu188Gln | |
| NM_001363729.2:c.562G>C | NP_001350658.1:p.Glu188Gln | |
| NM_001363733.2:c.562G>C | NP_001350662.1:p.Glu188Gln | |
| NM_015474.4:c.562G>C MANE Select | NP_056289.2:p.Glu188Gln |