Canonical Allele Identifier: CA2794333
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 349371
dbSNP Id: rs142802752
gnomAD v2: 4-650057-C-T
gnomAD v3: 4-656268-C-T
gnomAD v4: 4-656268-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.656268C>T , CM000666.2:g.656268C>T GRCh38
NC_000004.11:g.650057C>T , CM000666.1:g.650057C>T GRCh37
NC_000004.10:g.640057C>T NCBI36
NG_009839.1:g.35695C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496514.6:c.1083C>T MANE Select ENSP00000420295.1:p.Ser361=
ENST00000255622.10:c.1083C>T ENSP00000255622.6:p.Ser361=
ENST00000429163.6:c.246C>T ENSP00000406334.2:p.Ser82=
ENST00000487902.5:c.222+262C>T ENSP00000418256.1:n.222+262C>T
ENST00000496514.5:c.1083C>T ENSP00000420295.1:p.Ser361=
NM_000283.3:c.1083C>T NP_000274.2:p.Ser361=
NM_001145291.1:c.1083C>T NP_001138763.1:p.Ser361=
NM_001145292.1:c.246C>T NP_001138764.1:p.Ser82=
XM_011513473.1:c.1302C>T XP_011511775.1:p.Ser434=
XM_011513474.1:c.1302C>T XP_011511776.1:p.Ser434=
XM_011513475.1:c.1083C>T XP_011511777.1:p.Ser361=
XM_011513476.1:c.1302C>T XP_011511778.1:p.Ser434=
XM_011513477.1:c.288C>T XP_011511779.1:p.Ser96=
XM_011513478.1:c.12C>T XP_011511780.1:p.Ser4=
NM_001350154.1:c.246C>T NP_001337083.1:p.Ser82=
NM_001350155.1:c.-48-606C>T NP_001337084.1:n.-48-606C>T
XM_011513473.3:c.1302C>T XP_011511775.1:p.Ser434=
XM_011513474.3:c.1302C>T XP_011511776.1:p.Ser434=
XM_011513475.2:c.1083C>T XP_011511777.1:p.Ser361=
XM_011513476.3:c.1302C>T XP_011511778.1:p.Ser434=
XM_011513478.2:c.12C>T XP_011511780.1:p.Ser4=
XM_017008284.1:c.246C>T XP_016863773.1:p.Ser82=
XM_017008285.1:c.246C>T XP_016863774.1:p.Ser82=
XM_017008286.1:c.246C>T XP_016863775.1:p.Ser82=
NM_001350154.2:c.246C>T NP_001337083.1:p.Ser82=
NM_001350155.2:c.-48-606C>T NP_001337084.1:n.-48-606C>T
NM_000283.4:c.1083C>T MANE Select NP_000274.3:p.Ser361=
NM_001145291.2:c.1083C>T NP_001138763.2:p.Ser361=
NM_001145292.2:c.246C>T NP_001138764.2:p.Ser82=
NM_001350154.3:c.246C>T NP_001337083.1:p.Ser82=
NM_001350155.3:c.-48-606C>T NP_001337084.1:n.-48-606C>T
NM_001379246.1:c.246C>T NP_001366175.1:p.Ser82=
NM_001379247.1:c.246C>T NP_001366176.1:p.Ser82=