Linked Data
ClinVar Variation Id:
8913
dbSNP Id:
rs121434638
gnomAD v3:
11-1933737-G-A
gnomAD v4:
11-1933737-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1933737G>A , CM000673.2:g.1933737G>A | GRCh38 |
| NC_000011.9:g.1954967G>A , CM000673.1:g.1954967G>A | GRCh37 |
| NC_000011.8:g.1911543G>A | NCBI36 |
| NG_013085.1:g.19169G>A | |
| NG_013085.2:g.19169G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000706488.1:c.182G>A | ENSP00000516410.1:p.Arg61His | |
| ENST00000278317.11:c.188G>A MANE Select | ENSP00000278317.6:p.Arg63His | |
| ENST00000381558.6:c.164G>A | ENSP00000370970.1:p.Arg55His | |
| ENST00000639560.1:n.298G>A | ||
| ENST00000641119.1:c.182G>A | ENSP00000492914.1:p.Arg61His | |
| ENST00000641225.1:c.-17G>A | ENSP00000493372.1:n.-17G>A | |
| ENST00000641787.1:c.164G>A | ENSP00000493331.1:p.Arg55His | |
| ENST00000278317.10:c.188G>A | ENSP00000278317.6:p.Arg63His | |
| ENST00000344578.8:c.149G>A | ENSP00000344870.4:p.Arg50His | |
| ENST00000381557.6:c.146G>A | ENSP00000370969.2:p.Arg49His | |
| ENST00000381558.5:c.164G>A | ENSP00000370970.1:p.Arg55His | |
| ENST00000381563.8:c.197G>A | ENSP00000370975.4:p.Arg66His | |
| ENST00000381579.7:c.164G>A | ENSP00000370991.3:p.Arg55His | |
| ENST00000381589.7:c.182G>A | ENSP00000371001.3:p.Arg61His | |
| ENST00000397301.5:c.221G>A | ENSP00000380468.1:p.Arg74His | |
| ENST00000397304.6:c.131G>A | ENSP00000380471.2:p.Arg44His | |
| ENST00000446240.1:c.131G>A | ENSP00000413203.1:p.Arg44His | |
| ENST00000453458.5:c.131G>A | ENSP00000415614.1:p.Arg44His | |
| ENST00000492075.5:n.405G>A | ||
| NM_001042780.2:c.164G>A | NP_001036245.1:p.Arg55His | |
| NM_001042781.2:c.182G>A | NP_001036246.1:p.Arg61His | |
| NM_001042782.2:c.164G>A | NP_001036247.1:p.Arg55His | |
| NM_001297646.1:c.164G>A | NP_001284575.1:p.Arg55His | |
| NM_006757.3:c.188G>A | NP_006748.1:p.Arg63His | |
| XM_006718288.2:c.236G>A | XP_006718351.1:p.Arg79His | |
| XM_006718290.2:c.221G>A | XP_006718353.1:p.Arg74His | |
| XM_006718291.2:c.209G>A | XP_006718354.1:p.Arg70His | |
| XM_006718292.2:c.200G>A | XP_006718355.1:p.Arg67His | |
| XM_006718293.1:c.197G>A | XP_006718356.1:p.Arg66His | |
| XM_006718294.2:c.197G>A | XP_006718357.1:p.Arg66His | |
| XM_006718295.2:c.194G>A | XP_006718358.1:p.Arg65His | |
| XM_006718296.2:c.185G>A | XP_006718359.1:p.Arg62His | |
| XM_006718297.2:c.176G>A | XP_006718360.1:p.Arg59His | |
| XM_006718298.2:c.170G>A | XP_006718361.1:p.Arg57His | |
| XM_006718299.1:c.161G>A | XP_006718362.1:p.Arg54His | |
| XM_006718300.2:c.149G>A | XP_006718363.1:p.Arg50His | |
| XM_006718301.2:c.149G>A | XP_006718364.1:p.Arg50His | |
| XM_006718302.2:c.131G>A | XP_006718365.1:p.Arg44His | |
| XM_011520342.1:c.221G>A | XP_011518644.1:p.Arg74His | |
| XM_011520343.1:c.221G>A | XP_011518645.1:p.Arg74His | |
| NM_001363561.1:c.197G>A | NP_001350490.1:p.Arg66His | |
| XM_006718288.3:c.236G>A | XP_006718351.1:p.Arg79His | |
| XM_006718290.3:c.221G>A | XP_006718353.1:p.Arg74His | |
| XM_006718294.3:c.197G>A | XP_006718357.1:p.Arg66His | |
| XM_006718296.3:c.185G>A | XP_006718359.1:p.Arg62His | |
| XM_006718299.2:c.161G>A | XP_006718362.1:p.Arg54His | |
| XM_006718300.3:c.149G>A | XP_006718363.1:p.Arg50His | |
| XM_006718302.3:c.131G>A | XP_006718365.1:p.Arg44His | |
| XM_011520343.2:c.221G>A | XP_011518645.1:p.Arg74His | |
| XM_017018205.1:c.182G>A | XP_016873694.1:p.Arg61His | |
| XM_017018206.1:c.221G>A | XP_016873695.1:p.Arg74His | |
| XM_017018207.1:c.209G>A | XP_016873696.1:p.Arg70His | |
| XM_017018208.1:c.200G>A | XP_016873697.1:p.Arg67His | |
| XM_017018209.1:c.185G>A | XP_016873698.1:p.Arg62His | |
| XM_017018210.1:c.176G>A | XP_016873699.1:p.Arg59His | |
| XM_017018211.1:c.170G>A | XP_016873700.1:p.Arg57His | |
| XM_017018212.1:c.167G>A | XP_016873701.1:p.Arg56His | |
| XM_017018213.1:c.152G>A | XP_016873702.1:p.Arg51His | |
| XM_017018214.1:c.149G>A | XP_016873703.1:p.Arg50His | |
| XM_017018215.1:c.143G>A | XP_016873704.1:p.Arg48His | |
| XM_017018216.1:c.203G>A | XP_016873705.1:p.Arg68His | |
| XM_017018217.1:c.182G>A | XP_016873706.1:p.Arg61His | |
| XM_017018218.1:c.170G>A | XP_016873707.1:p.Arg57His | |
| XM_017018219.1:c.131G>A | XP_016873708.1:p.Arg44His | |
| XM_024448669.1:c.182G>A | XP_024304437.1:p.Arg61His | |
| XM_024448670.1:c.164G>A | XP_024304438.1:p.Arg55His | |
| XM_024448671.1:c.161G>A | XP_024304439.1:p.Arg54His | |
| XM_024448672.1:c.143G>A | XP_024304440.1:p.Arg48His | |
| NM_001367842.1:c.182G>A | NP_001354771.1:p.Arg61His | |
| NM_001367843.1:c.182G>A | NP_001354772.1:p.Arg61His | |
| NM_001367844.1:c.164G>A | NP_001354773.1:p.Arg55His | |
| NM_001367845.1:c.164G>A | NP_001354774.1:p.Arg55His | |
| NM_001367846.1:c.221G>A | NP_001354775.1:p.Arg74His | |
| NM_001367847.1:c.197G>A | NP_001354776.1:p.Arg66His | |
| NM_001367848.1:c.185G>A | NP_001354777.1:p.Arg62His | |
| NM_001367849.1:c.176G>A | NP_001354778.1:p.Arg59His | |
| NM_001367850.1:c.131G>A | NP_001354779.1:p.Arg44His | |
| NM_001367851.1:c.-17G>A | NP_001354780.1:n.-17G>A | |
| NM_001367852.1:c.-17G>A | NP_001354781.1:n.-17G>A | |
| NM_006757.4:c.188G>A MANE Select | NP_006748.1:p.Arg63His | |
| NM_001042780.3:c.164G>A | NP_001036245.1:p.Arg55His | |
| NM_001042781.3:c.182G>A | NP_001036246.1:p.Arg61His | |
| NM_001042782.3:c.164G>A | NP_001036247.1:p.Arg55His | |
| NM_001297646.2:c.164G>A | NP_001284575.1:p.Arg55His | |
| NM_001363561.2:c.197G>A | NP_001350490.1:p.Arg66His |