Linked Data
ClinVar Variation Id:
142445
dbSNP Id:
rs143965148
ExAC:
22:29085176 C / T
gnomAD v2:
22-29085176-C-T
gnomAD v3:
22-28689188-C-T
gnomAD v4:
22-28689188-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.28689188C>T , CM000684.2:g.28689188C>T | GRCh38 |
| NC_000022.10:g.29085176C>T , CM000684.1:g.29085176C>T | GRCh37 |
| NC_000022.9:g.27415176C>T | NCBI36 |
| NG_008150.1:g.57647G>A | |
| NG_008150.2:g.57679G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711048.1:c.*224G>A | ENSP00000518557.1:n.*224G>A | |
| ENST00000402731.6:c.1288G>A | ENSP00000384835.2:p.Asp430Asn | |
| ENST00000404276.6:c.1489G>A MANE Select | ENSP00000385747.1:p.Asp497Asn | |
| ENST00000425190.7:c.826G>A | ENSP00000390244.2:p.Asp276Asn | |
| ENST00000464581.6:c.829G>A | ENSP00000483777.2:p.Asp277Asn | |
| ENST00000648295.1:n.1041G>A | ||
| ENST00000649563.1:c.826G>A | ENSP00000496928.1:p.Asp276Asn | |
| ENST00000650281.1:c.1489G>A | ENSP00000497000.1:p.Asp497Asn | |
| ENST00000328354.10:c.1489G>A | ENSP00000329178.6:p.Asp497Asn | |
| ENST00000348295.7:c.1402G>A | ENSP00000329012.5:p.Asp468Asn | |
| ENST00000382580.6:c.1618G>A | ENSP00000372023.2:p.Asp540Asn | |
| ENST00000402731.5:c.1402G>A | ENSP00000384835.1:p.Asp468Asn | |
| ENST00000403642.5:c.1216G>A | ENSP00000384919.1:p.Asp406Asn | |
| ENST00000404276.5:c.1489G>A | ENSP00000385747.1:p.Asp497Asn | |
| ENST00000405598.5:c.1489G>A | ENSP00000386087.1:p.Asp497Asn | |
| ENST00000416671.5:c.*979G>A | ENSP00000402225.1:n.*979G>A | |
| ENST00000417588.5:c.1398G>A | ENSP00000412901.1:n.1398G>A | |
| ENST00000433728.5:c.1427G>A | ENSP00000404400.1:n.1427G>A | |
| ENST00000434810.5:c.687G>A | ||
| ENST00000448511.5:c.1379G>A | ENSP00000404567.1:n.1379G>A | |
| ENST00000456369.5:c.291G>A | ||
| ENST00000472807.1:n.223G>A | ||
| NM_001005735.1:c.1618G>A | NP_001005735.1:p.Asp540Asn | |
| NM_001257387.1:c.826G>A | NP_001244316.1:p.Asp276Asn | |
| NM_007194.3:c.1489G>A | NP_009125.1:p.Asp497Asn | |
| NM_145862.2:c.1402G>A | NP_665861.1:p.Asp468Asn | |
| XM_006724114.2:c.1009G>A | XP_006724177.1:p.Asp337Asn | |
| XM_006724116.2:c.946G>A | XP_006724179.2:p.Asp316Asn | |
| XM_011529839.1:c.1648G>A | XP_011528141.1:p.Asp550Asn | |
| XM_011529840.1:c.1561G>A | XP_011528142.1:p.Asp521Asn | |
| XM_011529841.1:c.1417G>A | XP_011528143.1:p.Asp473Asn | |
| XM_011529842.1:c.1318G>A | XP_011528144.1:p.Asp440Asn | |
| XM_011529843.1:c.1288G>A | XP_011528145.1:p.Asp430Asn | |
| XM_011529845.1:c.826G>A | XP_011528147.1:p.Asp276Asn | |
| XR_937805.1:n.1648G>A | ||
| NM_001349956.1:c.1288G>A | NP_001336885.1:p.Asp430Asn | |
| NM_007194.4:c.1489G>A MANE Select | NP_009125.1:p.Asp497Asn | |
| XM_006724114.3:c.1042G>A | XP_006724177.2:p.Asp348Asn | |
| XM_011529839.2:c.1648G>A | XP_011528141.1:p.Asp550Asn | |
| XM_011529840.3:c.1561G>A | XP_011528142.1:p.Asp521Asn | |
| XM_011529842.2:c.1318G>A | XP_011528144.1:p.Asp440Asn | |
| XM_011529845.2:c.826G>A | XP_011528147.1:p.Asp276Asn | |
| XM_017028560.1:c.1612G>A | XP_016884049.1:p.Asp538Asn | |
| XM_017028561.2:c.826G>A | XP_016884050.1:p.Asp276Asn | |
| XM_024452148.1:c.1519G>A | XP_024307916.1:p.Asp507Asn | |
| XM_024452149.1:c.1432G>A | XP_024307917.1:p.Asp478Asn | |
| XR_937805.2:n.1659G>A | ||
| NM_001005735.2:c.1618G>A | NP_001005735.1:p.Asp540Asn | |
| NM_001257387.2:c.826G>A | NP_001244316.1:p.Asp276Asn | |
| NM_001349956.2:c.1288G>A | NP_001336885.1:p.Asp430Asn |