Canonical Allele Identifier: CA1432844733

Gene: PDE6B PDE6B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.653967G= , CM000666.2:g.653967G=	GRCh38
NC_000004.11:g.647756G= , CM000666.1:g.647756G=	GRCh37
NC_000004.10:g.637756G=	NCBI36
NG_009839.1:g.33394G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.827G= (PDE6B) MANE Select	ENSP00000420295.1:p.Gly276=
ENST00000255622.10:c.827G= (PDE6B)	ENSP00000255622.6:p.Gly276=
ENST00000429163.6:c.-11G= (PDE6B)	ENSP00000406334.2:n.-11G=
ENST00000465426.5:c.-11G= (PDE6B)	ENSP00000418454.1:n.-11G=
ENST00000467152.1:n.225G= (PDE6B)
ENST00000474251.5:n.278G= (PDE6B)
ENST00000476034.5:n.397G= (PDE6B)
ENST00000487902.5:c.-11G= (PDE6B)	ENSP00000418256.1:n.-11G=
ENST00000488061.5:c.-11G= (PDE6B)	ENSP00000420228.1:n.-11G=
ENST00000496514.5:c.827G= (PDE6B)	ENSP00000420295.1:p.Gly276=
NM_000283.3:c.827G= (PDE6B)	NP_000274.2:p.Gly276=
NM_001145291.1:c.827G= (PDE6B)	NP_001138763.1:p.Gly276=
NM_001145292.1:c.-11G= (PDE6B)	NP_001138764.1:n.-11G=
XM_011513473.1:c.1046G= (PDE6B)	XP_011511775.1:p.Gly349=
XM_011513474.1:c.1046G= (PDE6B)	XP_011511776.1:p.Gly349=
XM_011513475.1:c.827G= (PDE6B)	XP_011511777.1:p.Gly276=
XM_011513476.1:c.1046G= (PDE6B)	XP_011511778.1:p.Gly349=
XM_011513477.1:c.-571G= (PDE6B)	XP_011511779.1:n.-571G=
XM_011513478.1:c.-914G= (PDE6B)	XP_011511780.1:n.-914G=
XR_246615.2:n.1019C= (PDE6B-AS1)
XR_925030.1:n.870C= (PDE6B-AS1)
NM_001350154.1:c.-11G= (PDE6B)	NP_001337083.1:n.-11G=
NM_001350155.1:c.-214G= (PDE6B)	NP_001337084.1:n.-214G=
XM_011513473.3:c.1046G= (PDE6B)	XP_011511775.1:p.Gly349=
XM_011513474.3:c.1046G= (PDE6B)	XP_011511776.1:p.Gly349=
XM_011513475.2:c.827G= (PDE6B)	XP_011511777.1:p.Gly276=
XM_011513476.3:c.1046G= (PDE6B)	XP_011511778.1:p.Gly349=
XM_011513478.2:c.-914G= (PDE6B)	XP_011511780.1:n.-914G=
XM_017008284.1:c.-11G= (PDE6B)	XP_016863773.1:n.-11G=
XM_017008285.1:c.-11G= (PDE6B)	XP_016863774.1:n.-11G=
XM_017008286.1:c.-11G= (PDE6B)	XP_016863775.1:n.-11G=
XR_001741541.1:n.1112C= (PDE6B-AS1)
XR_246615.3:n.1261C= (PDE6B-AS1)
NM_001350154.2:c.-11G= (PDE6B)	NP_001337083.1:n.-11G=
NM_001350155.2:c.-214G= (PDE6B)	NP_001337084.1:n.-214G=
NM_000283.4:c.827G= (PDE6B) MANE Select	NP_000274.3:p.Gly276=
NM_001145291.2:c.827G= (PDE6B)	NP_001138763.2:p.Gly276=
NM_001145292.2:c.-11G= (PDE6B)	NP_001138764.2:n.-11G=
NM_001350154.3:c.-11G= (PDE6B)	NP_001337083.1:n.-11G=
NM_001350155.3:c.-214G= (PDE6B)	NP_001337084.1:n.-214G=
NM_001379246.1:c.-11G= (PDE6B)	NP_001366175.1:n.-11G=
NM_001379247.1:c.-11G= (PDE6B)	NP_001366176.1:n.-11G=