Linked Data
ClinVar Variation Id:
220075
ClinVar RCV Id:
RCV001582710
dbSNP Id:
rs864622371
gnomAD v4:
22-28699846-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.28699846C>T , CM000684.2:g.28699846C>T | GRCh38 |
| NC_000022.10:g.29095834C>T , CM000684.1:g.29095834C>T | GRCh37 |
| NC_000022.9:g.27425834C>T | NCBI36 |
| NG_008150.1:g.46989G>A | |
| NG_008150.2:g.47021G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000439346.6:c.909G>A | ENSP00000396903.2:n.909G>A | |
| ENST00000711048.1:c.1000G>A | ENSP00000518557.1:p.Ala334Thr | |
| ENST00000402731.6:c.799G>A | ENSP00000384835.2:p.Ala267Thr | |
| ENST00000404276.6:c.1000G>A MANE Select | ENSP00000385747.1:p.Ala334Thr | |
| ENST00000425190.7:c.337G>A | ENSP00000390244.2:p.Ala113Thr | |
| ENST00000464581.6:c.340G>A | ENSP00000483777.2:p.Ala114Thr | |
| ENST00000648295.1:n.552G>A | ||
| ENST00000649563.1:c.337G>A | ENSP00000496928.1:p.Ala113Thr | |
| ENST00000650281.1:c.1000G>A | ENSP00000497000.1:p.Ala334Thr | |
| ENST00000328354.10:c.1000G>A | ENSP00000329178.6:p.Ala334Thr | |
| ENST00000348295.7:c.1000G>A | ENSP00000329012.5:p.Ala334Thr | |
| ENST00000382580.6:c.1129G>A | ENSP00000372023.2:p.Ala377Thr | |
| ENST00000402731.5:c.1000G>A | ENSP00000384835.1:p.Ala334Thr | |
| ENST00000403642.5:c.727G>A | ENSP00000384919.1:p.Ala243Thr | |
| ENST00000404276.5:c.1000G>A | ENSP00000385747.1:p.Ala334Thr | |
| ENST00000405598.5:c.1000G>A | ENSP00000386087.1:p.Ala334Thr | |
| ENST00000416671.5:c.*490G>A | ENSP00000402225.1:n.*490G>A | |
| ENST00000417588.5:c.909G>A | ENSP00000412901.1:n.909G>A | |
| ENST00000425190.6:c.337G>A | ENSP00000390244.1:p.Ala113Thr | |
| ENST00000433028.6:c.*725G>A | ENSP00000403659.1:n.*725G>A | |
| ENST00000433728.5:c.938G>A | ENSP00000404400.1:n.938G>A | |
| ENST00000434810.5:c.231G>A | ||
| ENST00000439346.5:c.471G>A | ENSP00000396903.1:n.471G>A | |
| ENST00000447421.5:c.799G>A | ENSP00000397478.2:p.Ala267Thr | |
| ENST00000448511.5:c.890G>A | ENSP00000404567.1:n.890G>A | |
| ENST00000456369.5:c.255G>A | ||
| ENST00000464581.5:c.340G>A | ENSP00000483777.1:p.Ala114Thr | |
| ENST00000491919.5:n.557G>A | ||
| NM_001005735.1:c.1129G>A | NP_001005735.1:p.Ala377Thr | |
| NM_001257387.1:c.337G>A | NP_001244316.1:p.Ala113Thr | |
| NM_007194.3:c.1000G>A | NP_009125.1:p.Ala334Thr | |
| NM_145862.2:c.1000G>A | NP_665861.1:p.Ala334Thr | |
| XM_006724114.2:c.520G>A | XP_006724177.1:p.Ala174Thr | |
| XM_006724116.2:c.457G>A | XP_006724179.2:p.Ala153Thr | |
| XM_011529839.1:c.1159G>A | XP_011528141.1:p.Ala387Thr | |
| XM_011529840.1:c.1159G>A | XP_011528142.1:p.Ala387Thr | |
| XM_011529841.1:c.928G>A | XP_011528143.1:p.Ala310Thr | |
| XM_011529842.1:c.829G>A | XP_011528144.1:p.Ala277Thr | |
| XM_011529843.1:c.799G>A | XP_011528145.1:p.Ala267Thr | |
| XM_011529844.1:c.1159G>A | XP_011528146.1:p.Ala387Thr | |
| XM_011529845.1:c.337G>A | XP_011528147.1:p.Ala113Thr | |
| XR_937805.1:n.1159G>A | ||
| XR_937806.1:n.1154G>A | ||
| XR_937807.1:n.1154G>A | ||
| NM_001349956.1:c.799G>A | NP_001336885.1:p.Ala267Thr | |
| NM_007194.4:c.1000G>A MANE Select | NP_009125.1:p.Ala334Thr | |
| XM_006724114.3:c.553G>A | XP_006724177.2:p.Ala185Thr | |
| XM_011529839.2:c.1159G>A | XP_011528141.1:p.Ala387Thr | |
| XM_011529840.3:c.1159G>A | XP_011528142.1:p.Ala387Thr | |
| XM_011529842.2:c.829G>A | XP_011528144.1:p.Ala277Thr | |
| XM_011529844.2:c.1159G>A | XP_011528146.1:p.Ala387Thr | |
| XM_011529845.2:c.337G>A | XP_011528147.1:p.Ala113Thr | |
| XM_017028560.1:c.1123G>A | XP_016884049.1:p.Ala375Thr | |
| XM_017028561.2:c.337G>A | XP_016884050.1:p.Ala113Thr | |
| XM_024452148.1:c.1030G>A | XP_024307916.1:p.Ala344Thr | |
| XM_024452149.1:c.1030G>A | XP_024307917.1:p.Ala344Thr | |
| XR_937805.2:n.1170G>A | ||
| XR_937806.2:n.1170G>A | ||
| XR_937807.2:n.1170G>A | ||
| NM_001005735.2:c.1129G>A | NP_001005735.1:p.Ala377Thr | |
| NM_001257387.2:c.337G>A | NP_001244316.1:p.Ala113Thr | |
| NM_001349956.2:c.799G>A | NP_001336885.1:p.Ala267Thr |