Canonical Allele Identifier: CA355916782

Gene: PDE6B

Linked Data

• MyVariant Identifiers: chr4:g.655941T>A (hg19) ; chr4:g.662152T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.662152T>A , CM000666.2:g.662152T>A	GRCh38
NC_000004.11:g.655941T>A , CM000666.1:g.655941T>A	GRCh37
NC_000004.10:g.645941T>A	NCBI36
NG_009839.1:g.41579T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1633T>A MANE Select	ENSP00000420295.1:p.Phe545Ile
ENST00000255622.10:c.1633T>A	ENSP00000255622.6:p.Phe545Ile
ENST00000429163.6:c.796T>A	ENSP00000406334.2:p.Phe266Ile
ENST00000496514.5:c.1633T>A	ENSP00000420295.1:p.Phe545Ile
NM_000283.3:c.1633T>A	NP_000274.2:p.Phe545Ile
NM_001145291.1:c.1633T>A	NP_001138763.1:p.Phe545Ile
NM_001145292.1:c.796T>A	NP_001138764.1:p.Phe266Ile
XM_011513473.1:c.1852T>A	XP_011511775.1:p.Phe618Ile
XM_011513474.1:c.1852T>A	XP_011511776.1:p.Phe618Ile
XM_011513475.1:c.1633T>A	XP_011511777.1:p.Phe545Ile
XM_011513476.1:c.1852T>A	XP_011511778.1:p.Phe618Ile
XM_011513477.1:c.838T>A	XP_011511779.1:p.Phe280Ile
XM_011513478.1:c.562T>A	XP_011511780.1:p.Phe188Ile
XR_925029.1:n.391A>T
NM_001350154.1:c.796T>A	NP_001337083.1:p.Phe266Ile
NM_001350155.1:c.478T>A	NP_001337084.1:p.Phe160Ile
XM_011513473.3:c.1852T>A	XP_011511775.1:p.Phe618Ile
XM_011513474.3:c.1852T>A	XP_011511776.1:p.Phe618Ile
XM_011513475.2:c.1633T>A	XP_011511777.1:p.Phe545Ile
XM_011513476.3:c.1852T>A	XP_011511778.1:p.Phe618Ile
XM_011513478.2:c.562T>A	XP_011511780.1:p.Phe188Ile
XM_017008284.1:c.796T>A	XP_016863773.1:p.Phe266Ile
XM_017008285.1:c.796T>A	XP_016863774.1:p.Phe266Ile
XM_017008286.1:c.796T>A	XP_016863775.1:p.Phe266Ile
NM_001350154.2:c.796T>A	NP_001337083.1:p.Phe266Ile
NM_001350155.2:c.478T>A	NP_001337084.1:p.Phe160Ile
NM_000283.4:c.1633T>A MANE Select	NP_000274.3:p.Phe545Ile
NM_001145291.2:c.1633T>A	NP_001138763.2:p.Phe545Ile
NM_001145292.2:c.796T>A	NP_001138764.2:p.Phe266Ile
NM_001350154.3:c.796T>A	NP_001337083.1:p.Phe266Ile
NM_001350155.3:c.478T>A	NP_001337084.1:p.Phe160Ile
NM_001379246.1:c.796T>A	NP_001366175.1:p.Phe266Ile
NM_001379247.1:c.796T>A	NP_001366176.1:p.Phe266Ile