Linked Data
ClinVar Variation Id:
136308
dbSNP Id:
rs181628906
ExAC:
22:40746045 C / T
gnomAD v2:
22-40746045-C-T
gnomAD v3:
22-40350041-C-T
gnomAD v4:
22-40350041-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.40350041C>T , CM000684.2:g.40350041C>T | GRCh38 |
| NC_000022.10:g.40746045C>T , CM000684.1:g.40746045C>T | GRCh37 |
| NC_000022.9:g.39075991C>T | NCBI36 |
| NG_007993.1:g.8542C>T | |
| NG_007993.2:g.8542C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480775.3:c.357+6C>T | ENSP00000485462.2:n.357+6C>T | |
| ENST00000623287.4:c.357+6C>T | ENSP00000485437.1:n.357+6C>T | |
| ENST00000623632.4:c.357+6C>T | ENSP00000485288.2:n.357+6C>T | |
| ENST00000625194.4:c.357+6C>T | ENSP00000485289.2:n.357+6C>T | |
| ENST00000636124.1:n.49+2689C>T | ||
| ENST00000636265.1:c.357+6C>T | ENSP00000490909.1:n.357+6C>T | |
| ENST00000636714.1:c.357+6C>T | ENSP00000490946.1:n.357+6C>T | |
| ENST00000637666.2:c.357+6C>T | ENSP00000489696.2:n.357+6C>T | |
| ENST00000637669.1:c.357+6C>T | ENSP00000489728.1:n.357+6C>T | |
| ENST00000638161.1:n.494+6C>T | ||
| ENST00000639722.1:c.*178+6C>T | ENSP00000492828.1:n.*178+6C>T | |
| ENST00000675622.1:n.393C>T | ||
| ENST00000679609.1:c.357+6C>T | ENSP00000506592.1:n.357+6C>T | |
| ENST00000679656.1:n.387+6C>T | ||
| ENST00000679723.1:c.357+6C>T | ENSP00000505155.1:n.357+6C>T | |
| ENST00000680378.1:c.357+6C>T | ENSP00000505556.1:n.357+6C>T | |
| ENST00000680444.1:c.357+6C>T | ENSP00000505298.1:n.357+6C>T | |
| ENST00000680978.1:c.357+6C>T | ENSP00000505244.1:n.357+6C>T | |
| ENST00000681159.1:n.416+6C>T | ||
| ENST00000216194.11:c.357+6C>T | ENSP00000216194.8:n.357+6C>T | |
| ENST00000342312.9:c.357+6C>T | ENSP00000341429.6:n.357+6C>T | |
| ENST00000466863.1:n.404C>T | ||
| ENST00000477111.2:n.387+6C>T | ||
| ENST00000623063.3:c.357+6C>T MANE Select | ENSP00000485525.1:n.357+6C>T | |
| ENST00000623287.3:c.357+6C>T | ENSP00000485437.1:n.357+6C>T | |
| ENST00000623632.3:c.357+6C>T | ENSP00000485288.1:n.357+6C>T | |
| ENST00000623978.3:c.-183-3032C>T | ENSP00000485477.1:n.-183-3032C>T | |
| ENST00000624474.1:c.357+6C>T | ENSP00000485286.1:n.357+6C>T | |
| ENST00000624503.1:c.363C>T | ENSP00000485073.1:p.Gly121= | |
| NM_000026.2:c.357+6C>T | NP_000017.1:n.357+6C>T | |
| NM_001123378.1:c.357+6C>T | NP_001116850.1:n.357+6C>T | |
| XM_011529976.1:c.357+6C>T | XP_011528278.1:n.357+6C>T | |
| XM_011529977.1:c.357+6C>T | XP_011528279.1:n.357+6C>T | |
| XM_011529978.1:c.357+6C>T | XP_011528280.1:n.357+6C>T | |
| XM_011529979.1:c.357+6C>T | XP_011528281.1:n.357+6C>T | |
| XM_011529980.1:c.357+6C>T | XP_011528282.1:n.357+6C>T | |
| XM_011529981.1:c.17+6C>T | XP_011528283.1:n.17+6C>T | |
| XR_937824.1:n.416+6C>T | ||
| XR_937825.1:n.416+6C>T | ||
| XR_937826.1:n.416+6C>T | ||
| NM_000026.3:c.357+6C>T | NP_000017.1:n.357+6C>T | |
| NM_001123378.2:c.357+6C>T | NP_001116850.1:n.357+6C>T | |
| NM_001317923.1:c.165+6C>T | NP_001304852.1:n.165+6C>T | |
| NM_001363840.1:c.357+6C>T | NP_001350769.1:n.357+6C>T | |
| NR_134256.1:n.416+6C>T | ||
| XM_011529977.3:c.357+6C>T | XP_011528279.1:n.357+6C>T | |
| XM_011529980.3:c.357+6C>T | XP_011528282.1:n.357+6C>T | |
| XM_017028636.1:c.357+6C>T | XP_016884125.1:n.357+6C>T | |
| XM_017028637.1:c.357+6C>T | XP_016884126.1:n.357+6C>T | |
| XM_017028638.1:c.17+6C>T | XP_016884127.1:n.17+6C>T | |
| XM_017028639.2:c.17+6C>T | XP_016884128.1:n.17+6C>T | |
| XM_024452166.1:c.357+6C>T | XP_024307934.1:n.357+6C>T | |
| XR_001755176.2:n.414+6C>T | ||
| XR_002958670.1:n.398+6C>T | ||
| XR_002958671.1:n.414+6C>T | ||
| XR_937825.3:n.414+6C>T | ||
| NM_000026.4:c.357+6C>T MANE Select | NP_000017.1:n.357+6C>T | |
| NM_001363840.2:c.357+6C>T | NP_001350769.1:n.357+6C>T | |
| NM_001123378.3:c.357+6C>T | NP_001116850.1:n.357+6C>T | |
| NM_001317923.2:c.165+6C>T | NP_001304852.1:n.165+6C>T | |
| NM_001363840.3:c.357+6C>T | NP_001350769.1:n.357+6C>T | |
| NR_134256.2:n.416+6C>T |