Linked Data
ClinVar Variation Id:
308941
dbSNP Id:
rs3803182
gnomAD v2:
12-48398223-G-A
gnomAD v3:
12-48004440-G-A
gnomAD v4:
12-48004440-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48004440G>A , CM000674.2:g.48004440G>A | GRCh38 |
| NC_000012.11:g.48398223G>A , CM000674.1:g.48398223G>A | GRCh37 |
| NC_000012.10:g.46684490G>A | NCBI36 |
| NG_008072.1:g.5063C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000337299.7:c.-119C>T | ENSP00000338213.6:n.-119C>T | |
| ENST00000380518.8:c.-119C>T MANE Select | ENSP00000369889.3:n.-119C>T | |
| ENST00000490609.2:n.115C>T | ||
| ENST00000380518.7:c.-119C>T | ENSP00000369889.3:n.-119C>T | |
| ENST00000474996.6:n.10C>T | ||
| ENST00000490609.1:n.47C>T | ||
| NM_001844.4:c.-119C>T | NP_001835.3:n.-119C>T | |
| NM_033150.2:c.-119C>T | NP_149162.2:n.-119C>T | |
| XM_006719242.2:c.166-143C>T | XP_006719305.2:n.166-143C>T | |
| XM_011537928.1:c.166-143C>T | XP_011536230.1:n.166-143C>T | |
| XM_011537929.1:c.166-143C>T | XP_011536231.1:n.166-143C>T | |
| XM_011537930.1:c.166-143C>T | XP_011536232.1:n.166-143C>T | |
| XM_011537931.1:c.166-143C>T | XP_011536233.1:n.166-143C>T | |
| XM_011537932.1:c.166-143C>T | XP_011536234.1:n.166-143C>T | |
| XM_011537933.1:c.166-143C>T | XP_011536235.1:n.166-143C>T | |
| XM_011537934.1:c.166-143C>T | XP_011536236.1:n.166-143C>T | |
| XM_017018828.1:c.166-143C>T | XP_016874317.1:n.166-143C>T | |
| XM_017018829.1:c.166-143C>T | XP_016874318.1:n.166-143C>T | |
| XM_017018830.1:c.166-143C>T | XP_016874319.1:n.166-143C>T | |
| NM_001844.5:c.-119C>T MANE Select | NP_001835.3:n.-119C>T | |
| NM_033150.3:c.-119C>T | NP_149162.2:n.-119C>T |