Linked Data
ClinVar Variation Id:
529216
dbSNP Id:
rs755359802
ExAC:
22:40754966 G / A
gnomAD v2:
22-40754966-G-A
gnomAD v4:
22-40358962-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.40358962G>A , CM000684.2:g.40358962G>A | GRCh38 |
| NC_000022.10:g.40754966G>A , CM000684.1:g.40754966G>A | GRCh37 |
| NC_000022.9:g.39084912G>A | NCBI36 |
| NG_007993.1:g.17463G>A | |
| NG_007993.2:g.17463G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480775.3:c.581G>A | ENSP00000485462.2:p.Arg194His | |
| ENST00000623287.4:c.*6G>A | ENSP00000485437.1:n.*6G>A | |
| ENST00000623632.4:c.581G>A | ENSP00000485288.2:p.Arg194His | |
| ENST00000625194.4:c.581G>A | ENSP00000485289.2:p.Arg194His | |
| ENST00000636124.1:n.273G>A | ||
| ENST00000636265.1:c.581G>A | ENSP00000490909.1:p.Arg194His | |
| ENST00000636433.1:n.603G>A | ||
| ENST00000636714.1:c.581G>A | ENSP00000490946.1:p.Arg194His | |
| ENST00000637666.2:c.581G>A | ENSP00000489696.2:p.Arg194His | |
| ENST00000637669.1:c.581G>A | ENSP00000489728.1:p.Arg194His | |
| ENST00000639722.1:c.*277G>A | ENSP00000492828.1:n.*277G>A | |
| ENST00000674592.1:n.605G>A | ||
| ENST00000675622.1:n.3648G>A | ||
| ENST00000679609.1:c.*6G>A | ENSP00000506592.1:n.*6G>A | |
| ENST00000679656.1:n.486G>A | ||
| ENST00000679723.1:c.536G>A | ENSP00000505155.1:p.Arg179His | |
| ENST00000679845.1:n.704G>A | ||
| ENST00000679904.1:n.568G>A | ||
| ENST00000680378.1:c.668G>A | ENSP00000505556.1:p.Arg223His | |
| ENST00000680444.1:c.581G>A | ENSP00000505298.1:p.Arg194His | |
| ENST00000680978.1:c.581G>A | ENSP00000505244.1:p.Arg194His | |
| ENST00000681159.1:n.640G>A | ||
| ENST00000216194.11:c.623G>A | ENSP00000216194.8:p.Arg208His | |
| ENST00000342312.9:c.581G>A | ENSP00000341429.6:p.Arg194His | |
| ENST00000477111.2:n.486G>A | ||
| ENST00000623063.3:c.581G>A MANE Select | ENSP00000485525.1:p.Arg194His | |
| ENST00000623287.3:c.*6G>A | ENSP00000485437.1:n.*6G>A | |
| ENST00000623632.3:c.536G>A | ENSP00000485288.1:p.Arg179His | |
| ENST00000623978.3:c.41G>A | ENSP00000485477.1:p.Arg14His | |
| ENST00000624474.1:c.*6G>A | ENSP00000485286.1:n.*6G>A | |
| ENST00000625194.3:c.168G>A | ||
| NM_000026.2:c.581G>A | NP_000017.1:p.Arg194His | |
| NM_001123378.1:c.581G>A | NP_001116850.1:p.Arg194His | |
| XM_011529976.1:c.581G>A | XP_011528278.1:p.Arg194His | |
| XM_011529977.1:c.581G>A | XP_011528279.1:p.Arg194His | |
| XM_011529978.1:c.581G>A | XP_011528280.1:p.Arg194His | |
| XM_011529979.1:c.581G>A | XP_011528281.1:p.Arg194His | |
| XM_011529980.1:c.581G>A | XP_011528282.1:p.Arg194His | |
| XM_011529981.1:c.116G>A | XP_011528283.1:p.Arg39His | |
| XR_937824.1:n.640G>A | ||
| XR_937825.1:n.640G>A | ||
| XR_937826.1:n.640G>A | ||
| NM_000026.3:c.581G>A | NP_000017.1:p.Arg194His | |
| NM_001123378.2:c.581G>A | NP_001116850.1:p.Arg194His | |
| NM_001317923.1:c.389G>A | NP_001304852.1:p.Arg130His | |
| NM_001363840.1:c.581G>A | NP_001350769.1:p.Arg194His | |
| NR_134256.1:n.640G>A | ||
| XM_011529977.3:c.581G>A | XP_011528279.1:p.Arg194His | |
| XM_011529980.3:c.581G>A | XP_011528282.1:p.Arg194His | |
| XM_017028636.1:c.536G>A | XP_016884125.1:p.Arg179His | |
| XM_017028637.1:c.536G>A | XP_016884126.1:p.Arg179His | |
| XM_017028638.1:c.116G>A | XP_016884127.1:p.Arg39His | |
| XM_017028639.2:c.116G>A | XP_016884128.1:p.Arg39His | |
| XM_024452166.1:c.536G>A | XP_024307934.1:p.Arg179His | |
| XR_001755176.2:n.638G>A | ||
| XR_002958670.1:n.577G>A | ||
| XR_002958671.1:n.638G>A | ||
| XR_937825.3:n.638G>A | ||
| NM_000026.4:c.581G>A MANE Select | NP_000017.1:p.Arg194His | |
| NM_001363840.2:c.581G>A | NP_001350769.1:p.Arg194His | |
| NM_001123378.3:c.581G>A | NP_001116850.1:p.Arg194His | |
| NM_001317923.2:c.389G>A | NP_001304852.1:p.Arg130His | |
| NM_001363840.3:c.581G>A | NP_001350769.1:p.Arg194His | |
| NR_134256.2:n.640G>A |