Canonical Allele Identifier: CA355911705

Gene: PDE6B PDE6B-AS1

Linked Data

• MyVariant Identifiers: chr4:g.647879A>C (hg19) ; chr4:g.654090A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.654090A>C , CM000666.2:g.654090A>C	GRCh38
NC_000004.11:g.647879A>C , CM000666.1:g.647879A>C	GRCh37
NC_000004.10:g.637879A>C	NCBI36
NG_009839.1:g.33517A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.863A>C (PDE6B) MANE Select	ENSP00000420295.1:p.Asp288Ala
ENST00000255622.10:c.863A>C (PDE6B)	ENSP00000255622.6:p.Asp288Ala
ENST00000429163.6:c.26A>C (PDE6B)	ENSP00000406334.2:p.Asp9Ala
ENST00000465426.5:c.26A>C (PDE6B)	ENSP00000418454.1:p.Asp9Ala
ENST00000467152.1:n.261A>C (PDE6B)
ENST00000474251.5:n.314A>C (PDE6B)
ENST00000476034.5:n.433A>C (PDE6B)
ENST00000487902.5:c.26A>C (PDE6B)	ENSP00000418256.1:p.Asp9Ala
ENST00000496514.5:c.863A>C (PDE6B)	ENSP00000420295.1:p.Asp288Ala
NM_000283.3:c.863A>C (PDE6B)	NP_000274.2:p.Asp288Ala
NM_001145291.1:c.863A>C (PDE6B)	NP_001138763.1:p.Asp288Ala
NM_001145292.1:c.26A>C (PDE6B)	NP_001138764.1:p.Asp9Ala
XM_011513473.1:c.1082A>C (PDE6B)	XP_011511775.1:p.Asp361Ala
XM_011513474.1:c.1082A>C (PDE6B)	XP_011511776.1:p.Asp361Ala
XM_011513475.1:c.863A>C (PDE6B)	XP_011511777.1:p.Asp288Ala
XM_011513476.1:c.1082A>C (PDE6B)	XP_011511778.1:p.Asp361Ala
XM_011513477.1:c.-535A>C (PDE6B)	XP_011511779.1:n.-535A>C
XM_011513478.1:c.-878A>C (PDE6B)	XP_011511780.1:n.-878A>C
XR_246615.2:n.989T>G (PDE6B-AS1)
XR_925030.1:n.866-119T>G (PDE6B-AS1)
NM_001350154.1:c.26A>C (PDE6B)	NP_001337083.1:p.Asp9Ala
NM_001350155.1:c.-178A>C (PDE6B)	NP_001337084.1:n.-178A>C
XM_011513473.3:c.1082A>C (PDE6B)	XP_011511775.1:p.Asp361Ala
XM_011513474.3:c.1082A>C (PDE6B)	XP_011511776.1:p.Asp361Ala
XM_011513475.2:c.863A>C (PDE6B)	XP_011511777.1:p.Asp288Ala
XM_011513476.3:c.1082A>C (PDE6B)	XP_011511778.1:p.Asp361Ala
XM_011513478.2:c.-878A>C (PDE6B)	XP_011511780.1:n.-878A>C
XM_017008284.1:c.26A>C (PDE6B)	XP_016863773.1:p.Asp9Ala
XM_017008285.1:c.26A>C (PDE6B)	XP_016863774.1:p.Asp9Ala
XM_017008286.1:c.26A>C (PDE6B)	XP_016863775.1:p.Asp9Ala
XR_001741541.1:n.1108-119T>G (PDE6B-AS1)
XR_246615.3:n.1231T>G (PDE6B-AS1)
NM_001350154.2:c.26A>C (PDE6B)	NP_001337083.1:p.Asp9Ala
NM_001350155.2:c.-178A>C (PDE6B)	NP_001337084.1:n.-178A>C
NM_000283.4:c.863A>C (PDE6B) MANE Select	NP_000274.3:p.Asp288Ala
NM_001145291.2:c.863A>C (PDE6B)	NP_001138763.2:p.Asp288Ala
NM_001145292.2:c.26A>C (PDE6B)	NP_001138764.2:p.Asp9Ala
NM_001350154.3:c.26A>C (PDE6B)	NP_001337083.1:p.Asp9Ala
NM_001350155.3:c.-178A>C (PDE6B)	NP_001337084.1:n.-178A>C
NM_001379246.1:c.26A>C (PDE6B)	NP_001366175.1:p.Asp9Ala
NM_001379247.1:c.26A>C (PDE6B)	NP_001366176.1:p.Asp9Ala