Linked Data
ClinVar Variation Id:
498723
dbSNP Id:
rs368166273
ExAC:
22:40750257 C / T
gnomAD v2:
22-40750257-C-T
gnomAD v3:
22-40354253-C-T
gnomAD v4:
22-40354253-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.40354253C>T , CM000684.2:g.40354253C>T | GRCh38 |
| NC_000022.10:g.40750257C>T , CM000684.1:g.40750257C>T | GRCh37 |
| NC_000022.9:g.39080203C>T | NCBI36 |
| NG_007993.1:g.12754C>T | |
| NG_007993.2:g.12754C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480775.3:c.408C>T | ENSP00000485462.2:p.Ala136= | |
| ENST00000623287.4:c.357+4218C>T | ENSP00000485437.1:n.357+4218C>T | |
| ENST00000623632.4:c.408C>T | ENSP00000485288.2:p.Ala136= | |
| ENST00000625194.4:c.408C>T | ENSP00000485289.2:p.Ala136= | |
| ENST00000636124.1:n.100C>T | ||
| ENST00000636265.1:c.408C>T | ENSP00000490909.1:p.Ala136= | |
| ENST00000636433.1:n.430C>T | ||
| ENST00000636714.1:c.408C>T | ENSP00000490946.1:p.Ala136= | |
| ENST00000637666.2:c.408C>T | ENSP00000489696.2:p.Ala136= | |
| ENST00000637669.1:c.408C>T | ENSP00000489728.1:p.Ala136= | |
| ENST00000638161.1:n.545C>T | ||
| ENST00000639722.1:c.*178+4218C>T | ENSP00000492828.1:n.*178+4218C>T | |
| ENST00000674592.1:n.432C>T | ||
| ENST00000675622.1:n.3475C>T | ||
| ENST00000679609.1:c.357+4218C>T | ENSP00000506592.1:n.357+4218C>T | |
| ENST00000679656.1:n.387+4218C>T | ||
| ENST00000679723.1:c.363C>T | ENSP00000505155.1:p.Ala121= | |
| ENST00000679845.1:n.531C>T | ||
| ENST00000679904.1:n.395C>T | ||
| ENST00000680378.1:c.495C>T | ENSP00000505556.1:p.Ala165= | |
| ENST00000680444.1:c.408C>T | ENSP00000505298.1:p.Ala136= | |
| ENST00000680978.1:c.408C>T | ENSP00000505244.1:p.Ala136= | |
| ENST00000681159.1:n.467C>T | ||
| ENST00000216194.11:c.450C>T | ENSP00000216194.8:p.Ala150= | |
| ENST00000342312.9:c.408C>T | ENSP00000341429.6:p.Ala136= | |
| ENST00000477111.2:n.387+4218C>T | ||
| ENST00000623063.3:c.408C>T MANE Select | ENSP00000485525.1:p.Ala136= | |
| ENST00000623287.3:c.357+4218C>T | ENSP00000485437.1:n.357+4218C>T | |
| ENST00000623632.3:c.363C>T | ENSP00000485288.1:p.Ala121= | |
| ENST00000623978.3:c.-133C>T | ENSP00000485477.1:n.-133C>T | |
| ENST00000624474.1:c.402+1136C>T | ENSP00000485286.1:n.402+1136C>T | |
| NM_000026.2:c.408C>T | NP_000017.1:p.Ala136= | |
| NM_001123378.1:c.408C>T | NP_001116850.1:p.Ala136= | |
| XM_011529976.1:c.408C>T | XP_011528278.1:p.Ala136= | |
| XM_011529977.1:c.408C>T | XP_011528279.1:p.Ala136= | |
| XM_011529978.1:c.408C>T | XP_011528280.1:p.Ala136= | |
| XM_011529979.1:c.408C>T | XP_011528281.1:p.Ala136= | |
| XM_011529980.1:c.408C>T | XP_011528282.1:p.Ala136= | |
| XM_011529981.1:c.17+4218C>T | XP_011528283.1:n.17+4218C>T | |
| XR_937824.1:n.467C>T | ||
| XR_937825.1:n.467C>T | ||
| XR_937826.1:n.467C>T | ||
| NM_000026.3:c.408C>T | NP_000017.1:p.Ala136= | |
| NM_001123378.2:c.408C>T | NP_001116850.1:p.Ala136= | |
| NM_001317923.1:c.216C>T | NP_001304852.1:p.Ala72= | |
| NM_001363840.1:c.408C>T | NP_001350769.1:p.Ala136= | |
| NR_134256.1:n.467C>T | ||
| XM_011529977.3:c.408C>T | XP_011528279.1:p.Ala136= | |
| XM_011529980.3:c.408C>T | XP_011528282.1:p.Ala136= | |
| XM_017028636.1:c.363C>T | XP_016884125.1:p.Ala121= | |
| XM_017028637.1:c.363C>T | XP_016884126.1:p.Ala121= | |
| XM_017028638.1:c.17+4218C>T | XP_016884127.1:n.17+4218C>T | |
| XM_017028639.2:c.17+4218C>T | XP_016884128.1:n.17+4218C>T | |
| XM_024452166.1:c.363C>T | XP_024307934.1:p.Ala121= | |
| XR_001755176.2:n.465C>T | ||
| XR_002958670.1:n.404C>T | ||
| XR_002958671.1:n.465C>T | ||
| XR_937825.3:n.465C>T | ||
| NM_000026.4:c.408C>T MANE Select | NP_000017.1:p.Ala136= | |
| NM_001363840.2:c.408C>T | NP_001350769.1:p.Ala136= | |
| NM_001123378.3:c.408C>T | NP_001116850.1:p.Ala136= | |
| NM_001317923.2:c.216C>T | NP_001304852.1:p.Ala72= | |
| NM_001363840.3:c.408C>T | NP_001350769.1:p.Ala136= | |
| NR_134256.2:n.467C>T |