Linked Data
ClinVar Variation Id:
497040
dbSNP Id:
rs370003608
ExAC:
8:144997036 G / A
gnomAD v2:
8-144997036-G-A
gnomAD v3:
8-143922868-G-A
gnomAD v4:
8-143922868-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143922868G>A , CM000670.2:g.143922868G>A | GRCh38 |
| NC_000008.10:g.144997036G>A , CM000670.1:g.144997036G>A | GRCh37 |
| NC_000008.9:g.145069024G>A | NCBI36 |
| NG_012492.1:g.58878C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.7193C>T | ENSP00000437303.2:p.Ala2398Val | |
| ENST00000685198.1:c.7112C>T | ENSP00000510528.1:p.Ala2371Val | |
| ENST00000687971.1:c.6779C>T | ENSP00000510788.1:p.Ala2260Val | |
| ENST00000693060.1:c.6992C>T | ENSP00000510329.1:p.Ala2331Val | |
| ENST00000345136.8:c.7061C>T MANE Select | ENSP00000344848.3:p.Ala2354Val | |
| ENST00000527303.2:c.4126-473C>T | ENSP00000433982.2:n.4126-473C>T | |
| ENST00000322810.8:c.7472C>T | ENSP00000323856.4:p.Ala2491Val | |
| ENST00000345136.7:c.7061C>T | ENSP00000344848.3:p.Ala2354Val | |
| ENST00000354589.7:c.7061C>T | ENSP00000346602.3:p.Ala2354Val | |
| ENST00000354958.6:c.6995C>T | ENSP00000347044.2:p.Ala2332Val | |
| ENST00000356346.7:c.7019C>T MANE Plus Clinical | ENSP00000348702.3:p.Ala2340Val | |
| ENST00000357649.6:c.7073C>T | ENSP00000350277.2:p.Ala2358Val | |
| ENST00000398774.6:c.6965C>T | ENSP00000381756.2:p.Ala2322Val | |
| ENST00000436759.6:c.7142C>T | ENSP00000388180.2:p.Ala2381Val | |
| ENST00000527096.5:c.7130C>T | ENSP00000434583.1:p.Ala2377Val | |
| ENST00000527303.1:c.135-473C>T | ||
| NM_000445.4:c.7142C>T | NP_000436.2:p.Ala2381Val | |
| NM_201378.3:c.7019C>T | NP_958780.1:p.Ala2340Val | |
| NM_201379.2:c.6995C>T | NP_958781.1:p.Ala2332Val | |
| NM_201380.3:c.7472C>T | NP_958782.1:p.Ala2491Val | |
| NM_201381.2:c.6965C>T | NP_958783.1:p.Ala2322Val | |
| NM_201382.3:c.7061C>T | NP_958784.1:p.Ala2354Val | |
| NM_201383.2:c.7073C>T | NP_958785.1:p.Ala2358Val | |
| NM_201384.2:c.7061C>T | NP_958786.1:p.Ala2354Val | |
| XM_005250976.2:c.7487C>T | XP_005251033.1:p.Ala2496Val | |
| XM_005250978.2:c.7088C>T | XP_005251035.1:p.Ala2363Val | |
| XM_005250979.3:c.7076C>T | XP_005251036.1:p.Ala2359Val | |
| XM_005250980.3:c.7076C>T | XP_005251037.1:p.Ala2359Val | |
| XM_005250981.2:c.7034C>T | XP_005251038.1:p.Ala2345Val | |
| XM_005250982.2:c.7010C>T | XP_005251039.1:p.Ala2337Val | |
| XM_005250983.2:c.6992C>T | XP_005251040.1:p.Ala2331Val | |
| XM_005250984.3:c.6980C>T | XP_005251041.1:p.Ala2327Val | |
| XM_006716588.2:c.7157C>T | XP_006716651.1:p.Ala2386Val | |
| XM_006716589.2:c.7007C>T | XP_006716652.1:p.Ala2336Val | |
| XM_006716590.2:c.7007C>T | XP_006716653.1:p.Ala2336Val | |
| XM_011517130.1:c.7076C>T | XP_011515432.1:p.Ala2359Val | |
| XM_011517131.1:c.6992C>T | XP_011515433.1:p.Ala2331Val | |
| XM_011517132.1:c.4072-473C>T | XP_011515434.1:n.4072-473C>T | |
| XM_005250976.4:c.7487C>T | XP_005251033.1:p.Ala2496Val | |
| XM_005250978.3:c.7088C>T | XP_005251035.1:p.Ala2363Val | |
| XM_005250979.4:c.7076C>T | XP_005251036.1:p.Ala2359Val | |
| XM_005250980.4:c.7076C>T | XP_005251037.1:p.Ala2359Val | |
| XM_005250981.3:c.7034C>T | XP_005251038.1:p.Ala2345Val | |
| XM_005250982.4:c.7010C>T | XP_005251039.1:p.Ala2337Val | |
| XM_005250984.5:c.6980C>T | XP_005251041.1:p.Ala2327Val | |
| XM_006716588.3:c.7157C>T | XP_006716651.1:p.Ala2386Val | |
| XM_006716590.3:c.7007C>T | XP_006716653.1:p.Ala2336Val | |
| XM_011517130.2:c.7076C>T | XP_011515432.1:p.Ala2359Val | |
| XM_011517131.2:c.6992C>T | XP_011515433.1:p.Ala2331Val | |
| XM_011517132.2:c.4072-473C>T | XP_011515434.1:n.4072-473C>T | |
| NM_000445.5:c.7142C>T | NP_000436.2:p.Ala2381Val | |
| NM_201378.4:c.7019C>T MANE Plus Clinical | NP_958780.1:p.Ala2340Val | |
| NM_201379.3:c.6995C>T | NP_958781.1:p.Ala2332Val | |
| NM_201380.4:c.7472C>T | NP_958782.1:p.Ala2491Val | |
| NM_201381.3:c.6965C>T | NP_958783.1:p.Ala2322Val | |
| NM_201382.4:c.7061C>T | NP_958784.1:p.Ala2354Val | |
| NM_201383.3:c.7073C>T | NP_958785.1:p.Ala2358Val | |
| NM_201384.3:c.7061C>T MANE Select | NP_958786.1:p.Ala2354Val |