Linked Data
ClinVar Variation Id:
13103
dbSNP Id:
rs121918579
ExAC:
4:647908 C / T
gnomAD v2:
4-647908-C-T
gnomAD v3:
4-654119-C-T
gnomAD v4:
4-654119-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.654119C>T , CM000666.2:g.654119C>T | GRCh38 |
| NC_000004.11:g.647908C>T , CM000666.1:g.647908C>T | GRCh37 |
| NC_000004.10:g.637908C>T | NCBI36 |
| NG_009839.1:g.33546C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496514.6:c.892C>T (PDE6B) MANE Select | ENSP00000420295.1:p.Gln298Ter | |
| ENST00000255622.10:c.892C>T (PDE6B) | ENSP00000255622.6:p.Gln298Ter | |
| ENST00000429163.6:c.55C>T (PDE6B) | ENSP00000406334.2:p.Gln19Ter | |
| ENST00000465426.5:c.55C>T (PDE6B) | ENSP00000418454.1:p.Gln19Ter | |
| ENST00000467152.1:n.290C>T (PDE6B) | ||
| ENST00000474251.5:n.343C>T (PDE6B) | ||
| ENST00000476034.5:n.462C>T (PDE6B) | ||
| ENST00000487902.5:c.55C>T (PDE6B) | ENSP00000418256.1:p.Gln19Ter | |
| ENST00000496514.5:c.892C>T (PDE6B) | ENSP00000420295.1:p.Gln298Ter | |
| NM_000283.3:c.892C>T (PDE6B) | NP_000274.2:p.Gln298Ter | |
| NM_001145291.1:c.892C>T (PDE6B) | NP_001138763.1:p.Gln298Ter | |
| NM_001145292.1:c.55C>T (PDE6B) | NP_001138764.1:p.Gln19Ter | |
| XM_011513473.1:c.1111C>T (PDE6B) | XP_011511775.1:p.Gln371Ter | |
| XM_011513474.1:c.1111C>T (PDE6B) | XP_011511776.1:p.Gln371Ter | |
| XM_011513475.1:c.892C>T (PDE6B) | XP_011511777.1:p.Gln298Ter | |
| XM_011513476.1:c.1111C>T (PDE6B) | XP_011511778.1:p.Gln371Ter | |
| XM_011513477.1:c.-506C>T (PDE6B) | XP_011511779.1:n.-506C>T | |
| XM_011513478.1:c.-849C>T (PDE6B) | XP_011511780.1:n.-849C>T | |
| XR_246615.2:n.960G>A (PDE6B-AS1) | ||
| XR_925030.1:n.866-148G>A (PDE6B-AS1) | ||
| NM_001350154.1:c.55C>T (PDE6B) | NP_001337083.1:p.Gln19Ter | |
| NM_001350155.1:c.-149C>T (PDE6B) | NP_001337084.1:n.-149C>T | |
| XM_011513473.3:c.1111C>T (PDE6B) | XP_011511775.1:p.Gln371Ter | |
| XM_011513474.3:c.1111C>T (PDE6B) | XP_011511776.1:p.Gln371Ter | |
| XM_011513475.2:c.892C>T (PDE6B) | XP_011511777.1:p.Gln298Ter | |
| XM_011513476.3:c.1111C>T (PDE6B) | XP_011511778.1:p.Gln371Ter | |
| XM_011513478.2:c.-849C>T (PDE6B) | XP_011511780.1:n.-849C>T | |
| XM_017008284.1:c.55C>T (PDE6B) | XP_016863773.1:p.Gln19Ter | |
| XM_017008285.1:c.55C>T (PDE6B) | XP_016863774.1:p.Gln19Ter | |
| XM_017008286.1:c.55C>T (PDE6B) | XP_016863775.1:p.Gln19Ter | |
| XR_001741541.1:n.1108-148G>A (PDE6B-AS1) | ||
| XR_246615.3:n.1202G>A (PDE6B-AS1) | ||
| NM_001350154.2:c.55C>T (PDE6B) | NP_001337083.1:p.Gln19Ter | |
| NM_001350155.2:c.-149C>T (PDE6B) | NP_001337084.1:n.-149C>T | |
| NM_000283.4:c.892C>T (PDE6B) MANE Select | NP_000274.3:p.Gln298Ter | |
| NM_001145291.2:c.892C>T (PDE6B) | NP_001138763.2:p.Gln298Ter | |
| NM_001145292.2:c.55C>T (PDE6B) | NP_001138764.2:p.Gln19Ter | |
| NM_001350154.3:c.55C>T (PDE6B) | NP_001337083.1:p.Gln19Ter | |
| NM_001350155.3:c.-149C>T (PDE6B) | NP_001337084.1:n.-149C>T | |
| NM_001379246.1:c.55C>T (PDE6B) | NP_001366175.1:p.Gln19Ter | |
| NM_001379247.1:c.55C>T (PDE6B) | NP_001366176.1:p.Gln19Ter |