Canonical Allele Identifier: CA1432844813

Gene: PDE6B PDE6B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.654022G= , CM000666.2:g.654022G=	GRCh38
NC_000004.11:g.647811G= , CM000666.1:g.647811G=	GRCh37
NC_000004.10:g.637811G=	NCBI36
NG_009839.1:g.33449G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496514.6:c.852+30G= (PDE6B) MANE Select	ENSP00000420295.1:n.852+30G=
ENST00000255622.10:c.852+30G= (PDE6B)	ENSP00000255622.6:n.852+30G=
ENST00000429163.6:c.15+30G= (PDE6B)	ENSP00000406334.2:n.15+30G=
ENST00000465426.5:c.15+30G= (PDE6B)	ENSP00000418454.1:n.15+30G=
ENST00000467152.1:n.250+30G= (PDE6B)
ENST00000474251.5:n.303+30G= (PDE6B)
ENST00000476034.5:n.422+30G= (PDE6B)
ENST00000487902.5:c.15+30G= (PDE6B)	ENSP00000418256.1:n.15+30G=
ENST00000488061.5:c.15+30G= (PDE6B)	ENSP00000420228.1:n.15+30G=
ENST00000496514.5:c.852+30G= (PDE6B)	ENSP00000420295.1:n.852+30G=
NM_000283.3:c.852+30G= (PDE6B)	NP_000274.2:n.852+30G=
NM_001145291.1:c.852+30G= (PDE6B)	NP_001138763.1:n.852+30G=
NM_001145292.1:c.15+30G= (PDE6B)	NP_001138764.1:n.15+30G=
XM_011513473.1:c.1071+30G= (PDE6B)	XP_011511775.1:n.1071+30G=
XM_011513474.1:c.1071+30G= (PDE6B)	XP_011511776.1:n.1071+30G=
XM_011513475.1:c.852+30G= (PDE6B)	XP_011511777.1:n.852+30G=
XM_011513476.1:c.1071+30G= (PDE6B)	XP_011511778.1:n.1071+30G=
XM_011513477.1:c.-546+30G= (PDE6B)	XP_011511779.1:n.-546+30G=
XM_011513478.1:c.-889+30G= (PDE6B)	XP_011511780.1:n.-889+30G=
XR_246615.2:n.1014+43C= (PDE6B-AS1)
XR_925030.1:n.866-51C= (PDE6B-AS1)
NM_001350154.1:c.15+30G= (PDE6B)	NP_001337083.1:n.15+30G=
NM_001350155.1:c.-189+30G= (PDE6B)	NP_001337084.1:n.-189+30G=
XM_011513473.3:c.1071+30G= (PDE6B)	XP_011511775.1:n.1071+30G=
XM_011513474.3:c.1071+30G= (PDE6B)	XP_011511776.1:n.1071+30G=
XM_011513475.2:c.852+30G= (PDE6B)	XP_011511777.1:n.852+30G=
XM_011513476.3:c.1071+30G= (PDE6B)	XP_011511778.1:n.1071+30G=
XM_011513478.2:c.-889+30G= (PDE6B)	XP_011511780.1:n.-889+30G=
XM_017008284.1:c.15+30G= (PDE6B)	XP_016863773.1:n.15+30G=
XM_017008285.1:c.15+30G= (PDE6B)	XP_016863774.1:n.15+30G=
XM_017008286.1:c.15+30G= (PDE6B)	XP_016863775.1:n.15+30G=
XR_001741541.1:n.1108-51C= (PDE6B-AS1)
XR_246615.3:n.1256+43C= (PDE6B-AS1)
NM_001350154.2:c.15+30G= (PDE6B)	NP_001337083.1:n.15+30G=
NM_001350155.2:c.-189+30G= (PDE6B)	NP_001337084.1:n.-189+30G=
NM_000283.4:c.852+30G= (PDE6B) MANE Select	NP_000274.3:n.852+30G=
NM_001145291.2:c.852+30G= (PDE6B)	NP_001138763.2:n.852+30G=
NM_001145292.2:c.15+30G= (PDE6B)	NP_001138764.2:n.15+30G=
NM_001350154.3:c.15+30G= (PDE6B)	NP_001337083.1:n.15+30G=
NM_001350155.3:c.-189+30G= (PDE6B)	NP_001337084.1:n.-189+30G=
NM_001379246.1:c.15+30G= (PDE6B)	NP_001366175.1:n.15+30G=
NM_001379247.1:c.15+30G= (PDE6B)	NP_001366176.1:n.15+30G=