Linked Data
ClinVar Variation Id:
432717
dbSNP Id:
rs199843296
ExAC:
8:145006576 T / A
gnomAD v2:
8-145006576-T-A
gnomAD v3:
8-143932408-T-A
gnomAD v4:
8-143932408-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143932408T>A , CM000670.2:g.143932408T>A | GRCh38 |
| NC_000008.10:g.145006576T>A , CM000670.1:g.145006576T>A | GRCh37 |
| NC_000008.9:g.145078564T>A | NCBI36 |
| NG_012492.1:g.49338A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.2101A>T | ENSP00000437303.2:p.Ser701Cys | |
| ENST00000685198.1:c.2020A>T | ENSP00000510528.1:p.Ser674Cys | |
| ENST00000687971.1:c.1687A>T | ENSP00000510788.1:p.Ser563Cys | |
| ENST00000693060.1:c.1900A>T | ENSP00000510329.1:p.Ser634Cys | |
| ENST00000345136.8:c.1969A>T MANE Select | ENSP00000344848.3:p.Ser657Cys | |
| ENST00000527303.2:c.2050A>T | ENSP00000433982.2:p.Ser684Cys | |
| ENST00000322810.8:c.2380A>T | ENSP00000323856.4:p.Ser794Cys | |
| ENST00000345136.7:c.1969A>T | ENSP00000344848.3:p.Ser657Cys | |
| ENST00000354589.7:c.1969A>T | ENSP00000346602.3:p.Ser657Cys | |
| ENST00000354958.6:c.1903A>T | ENSP00000347044.2:p.Ser635Cys | |
| ENST00000356346.7:c.1927A>T MANE Plus Clinical | ENSP00000348702.3:p.Ser643Cys | |
| ENST00000357649.6:c.1981A>T | ENSP00000350277.2:p.Ser661Cys | |
| ENST00000398774.6:c.1873A>T | ENSP00000381756.2:p.Ser625Cys | |
| ENST00000436759.6:c.2050A>T | ENSP00000388180.2:p.Ser684Cys | |
| ENST00000527096.5:c.2038A>T | ENSP00000434583.1:p.Ser680Cys | |
| ENST00000528025.5:c.2101A>T | ENSP00000437303.1:p.Ser701Cys | |
| NM_000445.4:c.2050A>T | NP_000436.2:p.Ser684Cys | |
| NM_201378.3:c.1927A>T | NP_958780.1:p.Ser643Cys | |
| NM_201379.2:c.1903A>T | NP_958781.1:p.Ser635Cys | |
| NM_201380.3:c.2380A>T | NP_958782.1:p.Ser794Cys | |
| NM_201381.2:c.1873A>T | NP_958783.1:p.Ser625Cys | |
| NM_201382.3:c.1969A>T | NP_958784.1:p.Ser657Cys | |
| NM_201383.2:c.1981A>T | NP_958785.1:p.Ser661Cys | |
| NM_201384.2:c.1969A>T | NP_958786.1:p.Ser657Cys | |
| XM_005250976.2:c.2395A>T | XP_005251033.1:p.Ser799Cys | |
| XM_005250978.2:c.1996A>T | XP_005251035.1:p.Ser666Cys | |
| XM_005250979.3:c.1984A>T | XP_005251036.1:p.Ser662Cys | |
| XM_005250980.3:c.1984A>T | XP_005251037.1:p.Ser662Cys | |
| XM_005250981.2:c.1942A>T | XP_005251038.1:p.Ser648Cys | |
| XM_005250982.2:c.1918A>T | XP_005251039.1:p.Ser640Cys | |
| XM_005250983.2:c.1900A>T | XP_005251040.1:p.Ser634Cys | |
| XM_005250984.3:c.1888A>T | XP_005251041.1:p.Ser630Cys | |
| XM_006716588.2:c.2065A>T | XP_006716651.1:p.Ser689Cys | |
| XM_006716589.2:c.1915A>T | XP_006716652.1:p.Ser639Cys | |
| XM_006716590.2:c.1915A>T | XP_006716653.1:p.Ser639Cys | |
| XM_011517130.1:c.1984A>T | XP_011515432.1:p.Ser662Cys | |
| XM_011517131.1:c.1900A>T | XP_011515433.1:p.Ser634Cys | |
| XM_011517132.1:c.1996A>T | XP_011515434.1:p.Ser666Cys | |
| XM_005250976.4:c.2395A>T | XP_005251033.1:p.Ser799Cys | |
| XM_005250978.3:c.1996A>T | XP_005251035.1:p.Ser666Cys | |
| XM_005250979.4:c.1984A>T | XP_005251036.1:p.Ser662Cys | |
| XM_005250980.4:c.1984A>T | XP_005251037.1:p.Ser662Cys | |
| XM_005250981.3:c.1942A>T | XP_005251038.1:p.Ser648Cys | |
| XM_005250982.4:c.1918A>T | XP_005251039.1:p.Ser640Cys | |
| XM_005250984.5:c.1888A>T | XP_005251041.1:p.Ser630Cys | |
| XM_006716588.3:c.2065A>T | XP_006716651.1:p.Ser689Cys | |
| XM_006716590.3:c.1915A>T | XP_006716653.1:p.Ser639Cys | |
| XM_011517130.2:c.1984A>T | XP_011515432.1:p.Ser662Cys | |
| XM_011517131.2:c.1900A>T | XP_011515433.1:p.Ser634Cys | |
| XM_011517132.2:c.1996A>T | XP_011515434.1:p.Ser666Cys | |
| NM_000445.5:c.2050A>T | NP_000436.2:p.Ser684Cys | |
| NM_201378.4:c.1927A>T MANE Plus Clinical | NP_958780.1:p.Ser643Cys | |
| NM_201379.3:c.1903A>T | NP_958781.1:p.Ser635Cys | |
| NM_201380.4:c.2380A>T | NP_958782.1:p.Ser794Cys | |
| NM_201381.3:c.1873A>T | NP_958783.1:p.Ser625Cys | |
| NM_201382.4:c.1969A>T | NP_958784.1:p.Ser657Cys | |
| NM_201383.3:c.1981A>T | NP_958785.1:p.Ser661Cys | |
| NM_201384.3:c.1969A>T MANE Select | NP_958786.1:p.Ser657Cys |