Linked Data
ClinVar Variation Id:
284581
dbSNP Id:
rs377039110
ExAC:
8:145006667 A / T
gnomAD v2:
8-145006667-A-T
gnomAD v3:
8-143932499-A-T
gnomAD v4:
8-143932499-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143932499A>T , CM000670.2:g.143932499A>T | GRCh38 |
| NC_000008.10:g.145006667A>T , CM000670.1:g.145006667A>T | GRCh37 |
| NC_000008.9:g.145078655A>T | NCBI36 |
| NG_012492.1:g.49247T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.2010T>A | ENSP00000437303.2:p.Thr670= | |
| ENST00000685198.1:c.1929T>A | ENSP00000510528.1:p.Thr643= | |
| ENST00000687971.1:c.1596T>A | ENSP00000510788.1:p.Thr532= | |
| ENST00000693060.1:c.1809T>A | ENSP00000510329.1:p.Thr603= | |
| ENST00000345136.8:c.1878T>A MANE Select | ENSP00000344848.3:p.Thr626= | |
| ENST00000527303.2:c.1959T>A | ENSP00000433982.2:p.Thr653= | |
| ENST00000322810.8:c.2289T>A | ENSP00000323856.4:p.Thr763= | |
| ENST00000345136.7:c.1878T>A | ENSP00000344848.3:p.Thr626= | |
| ENST00000354589.7:c.1878T>A | ENSP00000346602.3:p.Thr626= | |
| ENST00000354958.6:c.1812T>A | ENSP00000347044.2:p.Thr604= | |
| ENST00000356346.7:c.1836T>A MANE Plus Clinical | ENSP00000348702.3:p.Thr612= | |
| ENST00000357649.6:c.1890T>A | ENSP00000350277.2:p.Thr630= | |
| ENST00000398774.6:c.1782T>A | ENSP00000381756.2:p.Thr594= | |
| ENST00000436759.6:c.1959T>A | ENSP00000388180.2:p.Thr653= | |
| ENST00000527096.5:c.1947T>A | ENSP00000434583.1:p.Thr649= | |
| ENST00000528025.5:c.2010T>A | ENSP00000437303.1:p.Thr670= | |
| NM_000445.4:c.1959T>A | NP_000436.2:p.Thr653= | |
| NM_201378.3:c.1836T>A | NP_958780.1:p.Thr612= | |
| NM_201379.2:c.1812T>A | NP_958781.1:p.Thr604= | |
| NM_201380.3:c.2289T>A | NP_958782.1:p.Thr763= | |
| NM_201381.2:c.1782T>A | NP_958783.1:p.Thr594= | |
| NM_201382.3:c.1878T>A | NP_958784.1:p.Thr626= | |
| NM_201383.2:c.1890T>A | NP_958785.1:p.Thr630= | |
| NM_201384.2:c.1878T>A | NP_958786.1:p.Thr626= | |
| XM_005250976.2:c.2304T>A | XP_005251033.1:p.Thr768= | |
| XM_005250978.2:c.1905T>A | XP_005251035.1:p.Thr635= | |
| XM_005250979.3:c.1893T>A | XP_005251036.1:p.Thr631= | |
| XM_005250980.3:c.1893T>A | XP_005251037.1:p.Thr631= | |
| XM_005250981.2:c.1851T>A | XP_005251038.1:p.Thr617= | |
| XM_005250982.2:c.1827T>A | XP_005251039.1:p.Thr609= | |
| XM_005250983.2:c.1809T>A | XP_005251040.1:p.Thr603= | |
| XM_005250984.3:c.1797T>A | XP_005251041.1:p.Thr599= | |
| XM_006716588.2:c.1974T>A | XP_006716651.1:p.Thr658= | |
| XM_006716589.2:c.1824T>A | XP_006716652.1:p.Thr608= | |
| XM_006716590.2:c.1824T>A | XP_006716653.1:p.Thr608= | |
| XM_011517130.1:c.1893T>A | XP_011515432.1:p.Thr631= | |
| XM_011517131.1:c.1809T>A | XP_011515433.1:p.Thr603= | |
| XM_011517132.1:c.1905T>A | XP_011515434.1:p.Thr635= | |
| XM_005250976.4:c.2304T>A | XP_005251033.1:p.Thr768= | |
| XM_005250978.3:c.1905T>A | XP_005251035.1:p.Thr635= | |
| XM_005250979.4:c.1893T>A | XP_005251036.1:p.Thr631= | |
| XM_005250980.4:c.1893T>A | XP_005251037.1:p.Thr631= | |
| XM_005250981.3:c.1851T>A | XP_005251038.1:p.Thr617= | |
| XM_005250982.4:c.1827T>A | XP_005251039.1:p.Thr609= | |
| XM_005250984.5:c.1797T>A | XP_005251041.1:p.Thr599= | |
| XM_006716588.3:c.1974T>A | XP_006716651.1:p.Thr658= | |
| XM_006716590.3:c.1824T>A | XP_006716653.1:p.Thr608= | |
| XM_011517130.2:c.1893T>A | XP_011515432.1:p.Thr631= | |
| XM_011517131.2:c.1809T>A | XP_011515433.1:p.Thr603= | |
| XM_011517132.2:c.1905T>A | XP_011515434.1:p.Thr635= | |
| NM_000445.5:c.1959T>A | NP_000436.2:p.Thr653= | |
| NM_201378.4:c.1836T>A MANE Plus Clinical | NP_958780.1:p.Thr612= | |
| NM_201379.3:c.1812T>A | NP_958781.1:p.Thr604= | |
| NM_201380.4:c.2289T>A | NP_958782.1:p.Thr763= | |
| NM_201381.3:c.1782T>A | NP_958783.1:p.Thr594= | |
| NM_201382.4:c.1878T>A | NP_958784.1:p.Thr626= | |
| NM_201383.3:c.1890T>A | NP_958785.1:p.Thr630= | |
| NM_201384.3:c.1878T>A MANE Select | NP_958786.1:p.Thr626= |