Linked Data
ClinVar Variation Id:
527836
dbSNP Id:
rs757841535
ExAC:
19:1218423 C / G
gnomAD v2:
19-1218423-C-G
gnomAD v3:
19-1218424-C-G
gnomAD v4:
19-1218424-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1218424C>G , CM000681.2:g.1218424C>G | GRCh38 |
| NC_000019.9:g.1218423C>G , CM000681.1:g.1218423C>G | GRCh37 |
| NC_000019.8:g.1169423C>G | NCBI36 |
| NG_007460.2:g.34018C>G , LRG_319:g.34018C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.298C>G | ENSP00000490268.2:p.Gln100Glu | |
| ENST00000585748.3:c.-75C>G | ENSP00000477641.2:n.-75C>G | |
| ENST00000585851.2:c.291-1949C>G | ENSP00000467912.2:n.291-1949C>G | |
| ENST00000326873.12:c.298C>G MANE Select | ENSP00000324856.6:p.Gln100Glu | |
| ENST00000652231.1:c.298C>G | ENSP00000498804.1:p.Gln100Glu | |
| ENST00000326873.11:c.298C>G | ENSP00000324856.6:p.Gln100Glu | |
| ENST00000585748.2:c.-75C>G | ENSP00000477641.1:n.-75C>G | |
| ENST00000585851.1:c.291-1949C>G | ENSP00000467912.1:n.291-1949C>G | |
| ENST00000586243.5:c.298C>G | ENSP00000467240.2:p.Gln100Glu | |
| ENST00000586358.5:n.121C>G | ||
| ENST00000589152.5:n.388C>G | ||
| ENST00000593219.5:c.*123C>G | ENSP00000466610.1:n.*123C>G | |
| NM_000455.4:c.298C>G , LRG_319t1:c.298C>G | NP_000446.1:p.Gln100Glu | |
| XM_005259617.1:c.298C>G | XP_005259674.1:p.Gln100Glu | |
| XM_005259618.3:c.298C>G | XP_005259675.1:p.Gln100Glu | |
| XM_011528209.1:c.76C>G | XP_011526511.1:p.Gln26Glu | |
| XR_936204.1:n.923C>G | ||
| XM_005259617.3:c.298C>G | XP_005259674.1:p.Gln100Glu | |
| XM_011528209.2:c.76C>G | XP_011526511.1:p.Gln26Glu | |
| XR_001753738.2:n.923C>G | ||
| XR_001753739.1:n.923C>G | ||
| XR_001753740.2:n.923C>G | ||
| NM_000455.5:c.298C>G MANE Select | NP_000446.1:p.Gln100Glu |