Canonical Allele Identifier: CA355916739
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 2195451
ClinVar RCV Id: RCV002628677
dbSNP Id: rs1319627398
gnomAD v4: 4-662140-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.662140G>A , CM000666.2:g.662140G>A GRCh38
NC_000004.11:g.655929G>A , CM000666.1:g.655929G>A GRCh37
NC_000004.10:g.645929G>A NCBI36
NG_009839.1:g.41567G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496514.6:c.1621G>A MANE Select ENSP00000420295.1:p.Val541Met
ENST00000255622.10:c.1621G>A ENSP00000255622.6:p.Val541Met
ENST00000429163.6:c.784G>A ENSP00000406334.2:p.Val262Met
ENST00000496514.5:c.1621G>A ENSP00000420295.1:p.Val541Met
NM_000283.3:c.1621G>A NP_000274.2:p.Val541Met
NM_001145291.1:c.1621G>A NP_001138763.1:p.Val541Met
NM_001145292.1:c.784G>A NP_001138764.1:p.Val262Met
XM_011513473.1:c.1840G>A XP_011511775.1:p.Val614Met
XM_011513474.1:c.1840G>A XP_011511776.1:p.Val614Met
XM_011513475.1:c.1621G>A XP_011511777.1:p.Val541Met
XM_011513476.1:c.1840G>A XP_011511778.1:p.Val614Met
XM_011513477.1:c.826G>A XP_011511779.1:p.Val276Met
XM_011513478.1:c.550G>A XP_011511780.1:p.Val184Met
XR_925029.1:n.403C>T
NM_001350154.1:c.784G>A NP_001337083.1:p.Val262Met
NM_001350155.1:c.466G>A NP_001337084.1:p.Val156Met
XM_011513473.3:c.1840G>A XP_011511775.1:p.Val614Met
XM_011513474.3:c.1840G>A XP_011511776.1:p.Val614Met
XM_011513475.2:c.1621G>A XP_011511777.1:p.Val541Met
XM_011513476.3:c.1840G>A XP_011511778.1:p.Val614Met
XM_011513478.2:c.550G>A XP_011511780.1:p.Val184Met
XM_017008284.1:c.784G>A XP_016863773.1:p.Val262Met
XM_017008285.1:c.784G>A XP_016863774.1:p.Val262Met
XM_017008286.1:c.784G>A XP_016863775.1:p.Val262Met
NM_001350154.2:c.784G>A NP_001337083.1:p.Val262Met
NM_001350155.2:c.466G>A NP_001337084.1:p.Val156Met
NM_000283.4:c.1621G>A MANE Select NP_000274.3:p.Val541Met
NM_001145291.2:c.1621G>A NP_001138763.2:p.Val541Met
NM_001145292.2:c.784G>A NP_001138764.2:p.Val262Met
NM_001350154.3:c.784G>A NP_001337083.1:p.Val262Met
NM_001350155.3:c.466G>A NP_001337084.1:p.Val156Met
NM_001379246.1:c.784G>A NP_001366175.1:p.Val262Met
NM_001379247.1:c.784G>A NP_001366176.1:p.Val262Met