Linked Data
ClinVar Variation Id:
349363
dbSNP Id:
rs138789637
ExAC:
4:647718 G / A
gnomAD v2:
4-647718-G-A
gnomAD v3:
4-653929-G-A
gnomAD v4:
4-653929-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.653929G>A , CM000666.2:g.653929G>A | GRCh38 |
| NC_000004.11:g.647718G>A , CM000666.1:g.647718G>A | GRCh37 |
| NC_000004.10:g.637718G>A | NCBI36 |
| NG_009839.1:g.33356G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496514.6:c.789G>A (PDE6B) MANE Select | ENSP00000420295.1:p.Thr263= | |
| ENST00000255622.10:c.789G>A (PDE6B) | ENSP00000255622.6:p.Thr263= | |
| ENST00000429163.6:c.-49G>A (PDE6B) | ENSP00000406334.2:n.-49G>A | |
| ENST00000465426.5:c.-49G>A (PDE6B) | ENSP00000418454.1:n.-49G>A | |
| ENST00000467152.1:n.187G>A (PDE6B) | ||
| ENST00000474251.5:n.240G>A (PDE6B) | ||
| ENST00000476034.5:n.359G>A (PDE6B) | ||
| ENST00000487902.5:c.-49G>A (PDE6B) | ENSP00000418256.1:n.-49G>A | |
| ENST00000488061.5:c.-49G>A (PDE6B) | ENSP00000420228.1:n.-49G>A | |
| ENST00000496514.5:c.789G>A (PDE6B) | ENSP00000420295.1:p.Thr263= | |
| NM_000283.3:c.789G>A (PDE6B) | NP_000274.2:p.Thr263= | |
| NM_001145291.1:c.789G>A (PDE6B) | NP_001138763.1:p.Thr263= | |
| NM_001145292.1:c.-49G>A (PDE6B) | NP_001138764.1:n.-49G>A | |
| XM_011513473.1:c.1008G>A (PDE6B) | XP_011511775.1:p.Thr336= | |
| XM_011513474.1:c.1008G>A (PDE6B) | XP_011511776.1:p.Thr336= | |
| XM_011513475.1:c.789G>A (PDE6B) | XP_011511777.1:p.Thr263= | |
| XM_011513476.1:c.1008G>A (PDE6B) | XP_011511778.1:p.Thr336= | |
| XM_011513477.1:c.-609G>A (PDE6B) | XP_011511779.1:n.-609G>A | |
| XM_011513478.1:c.-952G>A (PDE6B) | XP_011511780.1:n.-952G>A | |
| XR_246615.2:n.1057C>T (PDE6B-AS1) | ||
| XR_925030.1:n.908C>T (PDE6B-AS1) | ||
| NM_001350154.1:c.-49G>A (PDE6B) | NP_001337083.1:n.-49G>A | |
| NM_001350155.1:c.-252G>A (PDE6B) | NP_001337084.1:n.-252G>A | |
| XM_011513473.3:c.1008G>A (PDE6B) | XP_011511775.1:p.Thr336= | |
| XM_011513474.3:c.1008G>A (PDE6B) | XP_011511776.1:p.Thr336= | |
| XM_011513475.2:c.789G>A (PDE6B) | XP_011511777.1:p.Thr263= | |
| XM_011513476.3:c.1008G>A (PDE6B) | XP_011511778.1:p.Thr336= | |
| XM_011513478.2:c.-952G>A (PDE6B) | XP_011511780.1:n.-952G>A | |
| XM_017008284.1:c.-49G>A (PDE6B) | XP_016863773.1:n.-49G>A | |
| XM_017008285.1:c.-49G>A (PDE6B) | XP_016863774.1:n.-49G>A | |
| XM_017008286.1:c.-49G>A (PDE6B) | XP_016863775.1:n.-49G>A | |
| XR_001741541.1:n.1150C>T (PDE6B-AS1) | ||
| XR_246615.3:n.1299C>T (PDE6B-AS1) | ||
| NM_001350154.2:c.-49G>A (PDE6B) | NP_001337083.1:n.-49G>A | |
| NM_001350155.2:c.-252G>A (PDE6B) | NP_001337084.1:n.-252G>A | |
| NM_000283.4:c.789G>A (PDE6B) MANE Select | NP_000274.3:p.Thr263= | |
| NM_001145291.2:c.789G>A (PDE6B) | NP_001138763.2:p.Thr263= | |
| NM_001145292.2:c.-49G>A (PDE6B) | NP_001138764.2:n.-49G>A | |
| NM_001350154.3:c.-49G>A (PDE6B) | NP_001337083.1:n.-49G>A | |
| NM_001350155.3:c.-252G>A (PDE6B) | NP_001337084.1:n.-252G>A | |
| NM_001379246.1:c.-49G>A (PDE6B) | NP_001366175.1:n.-49G>A | |
| NM_001379247.1:c.-49G>A (PDE6B) | NP_001366176.1:n.-49G>A |