Linked Data
ClinVar Variation Id:
282486
dbSNP Id:
rs189859084
ExAC:
8:144993480 C / T
gnomAD v2:
8-144993480-C-T
gnomAD v3:
8-143919312-C-T
gnomAD v4:
8-143919312-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143919312C>T , CM000670.2:g.143919312C>T | GRCh38 |
| NC_000008.10:g.144993480C>T , CM000670.1:g.144993480C>T | GRCh37 |
| NC_000008.9:g.145065468C>T | NCBI36 |
| NG_012492.1:g.62434G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.10641G>A | ENSP00000437303.2:p.Ala3547= | |
| ENST00000685198.1:c.10560G>A | ENSP00000510528.1:p.Ala3520= | |
| ENST00000687971.1:c.10227G>A | ENSP00000510788.1:p.Ala3409= | |
| ENST00000693060.1:c.10440G>A | ENSP00000510329.1:p.Ala3480= | |
| ENST00000345136.8:c.10509G>A MANE Select | ENSP00000344848.3:p.Ala3503= | |
| ENST00000527303.2:c.7209G>A | ENSP00000433982.2:p.Ala2403= | |
| ENST00000322810.8:c.10920G>A | ENSP00000323856.4:p.Ala3640= | |
| ENST00000345136.7:c.10509G>A | ENSP00000344848.3:p.Ala3503= | |
| ENST00000354589.7:c.10509G>A | ENSP00000346602.3:p.Ala3503= | |
| ENST00000354958.6:c.10443G>A | ENSP00000347044.2:p.Ala3481= | |
| ENST00000356346.7:c.10467G>A MANE Plus Clinical | ENSP00000348702.3:p.Ala3489= | |
| ENST00000357649.6:c.10521G>A | ENSP00000350277.2:p.Ala3507= | |
| ENST00000398774.6:c.10413G>A | ENSP00000381756.2:p.Ala3471= | |
| ENST00000436759.6:c.10590G>A | ENSP00000388180.2:p.Ala3530= | |
| ENST00000527096.5:c.10578G>A | ENSP00000434583.1:p.Ala3526= | |
| NM_000445.4:c.10590G>A | NP_000436.2:p.Ala3530= | |
| NM_201378.3:c.10467G>A | NP_958780.1:p.Ala3489= | |
| NM_201379.2:c.10443G>A | NP_958781.1:p.Ala3481= | |
| NM_201380.3:c.10920G>A | NP_958782.1:p.Ala3640= | |
| NM_201381.2:c.10413G>A | NP_958783.1:p.Ala3471= | |
| NM_201382.3:c.10509G>A | NP_958784.1:p.Ala3503= | |
| NM_201383.2:c.10521G>A | NP_958785.1:p.Ala3507= | |
| NM_201384.2:c.10509G>A | NP_958786.1:p.Ala3503= | |
| XM_005250976.2:c.10935G>A | XP_005251033.1:p.Ala3645= | |
| XM_005250978.2:c.10536G>A | XP_005251035.1:p.Ala3512= | |
| XM_005250979.3:c.10524G>A | XP_005251036.1:p.Ala3508= | |
| XM_005250980.3:c.10524G>A | XP_005251037.1:p.Ala3508= | |
| XM_005250981.2:c.10482G>A | XP_005251038.1:p.Ala3494= | |
| XM_005250982.2:c.10458G>A | XP_005251039.1:p.Ala3486= | |
| XM_005250983.2:c.10440G>A | XP_005251040.1:p.Ala3480= | |
| XM_005250984.3:c.10428G>A | XP_005251041.1:p.Ala3476= | |
| XM_006716588.2:c.10605G>A | XP_006716651.1:p.Ala3535= | |
| XM_006716589.2:c.10455G>A | XP_006716652.1:p.Ala3485= | |
| XM_006716590.2:c.10455G>A | XP_006716653.1:p.Ala3485= | |
| XM_011517130.1:c.10524G>A | XP_011515432.1:p.Ala3508= | |
| XM_011517131.1:c.10440G>A | XP_011515433.1:p.Ala3480= | |
| XM_011517132.1:c.7155G>A | XP_011515434.1:p.Ala2385= | |
| XM_005250976.4:c.10935G>A | XP_005251033.1:p.Ala3645= | |
| XM_005250978.3:c.10536G>A | XP_005251035.1:p.Ala3512= | |
| XM_005250979.4:c.10524G>A | XP_005251036.1:p.Ala3508= | |
| XM_005250980.4:c.10524G>A | XP_005251037.1:p.Ala3508= | |
| XM_005250981.3:c.10482G>A | XP_005251038.1:p.Ala3494= | |
| XM_005250982.4:c.10458G>A | XP_005251039.1:p.Ala3486= | |
| XM_005250984.5:c.10428G>A | XP_005251041.1:p.Ala3476= | |
| XM_006716588.3:c.10605G>A | XP_006716651.1:p.Ala3535= | |
| XM_006716590.3:c.10455G>A | XP_006716653.1:p.Ala3485= | |
| XM_011517130.2:c.10524G>A | XP_011515432.1:p.Ala3508= | |
| XM_011517131.2:c.10440G>A | XP_011515433.1:p.Ala3480= | |
| XM_011517132.2:c.7155G>A | XP_011515434.1:p.Ala2385= | |
| NM_000445.5:c.10590G>A | NP_000436.2:p.Ala3530= | |
| NM_201378.4:c.10467G>A MANE Plus Clinical | NP_958780.1:p.Ala3489= | |
| NM_201379.3:c.10443G>A | NP_958781.1:p.Ala3481= | |
| NM_201380.4:c.10920G>A | NP_958782.1:p.Ala3640= | |
| NM_201381.3:c.10413G>A | NP_958783.1:p.Ala3471= | |
| NM_201382.4:c.10509G>A | NP_958784.1:p.Ala3503= | |
| NM_201383.3:c.10521G>A | NP_958785.1:p.Ala3507= | |
| NM_201384.3:c.10509G>A MANE Select | NP_958786.1:p.Ala3503= |