Canonical Allele Identifier: CA1432859229

Gene: PDE6B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.662201A= , CM000666.2:g.662201A=	GRCh38
NC_000004.11:g.655990A= , CM000666.1:g.655990A=	GRCh37
NC_000004.10:g.645990A=	NCBI36
NG_009839.1:g.41628A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1682A= MANE Select	ENSP00000420295.1:p.His561=
ENST00000255622.10:c.1682A=	ENSP00000255622.6:p.His561=
ENST00000429163.6:c.845A=	ENSP00000406334.2:p.His282=
ENST00000496514.5:c.1682A=	ENSP00000420295.1:p.His561=
NM_000283.3:c.1682A=	NP_000274.2:p.His561=
NM_001145291.1:c.1682A=	NP_001138763.1:p.His561=
NM_001145292.1:c.845A=	NP_001138764.1:p.His282=
XM_011513473.1:c.1901A=	XP_011511775.1:p.His634=
XM_011513474.1:c.1901A=	XP_011511776.1:p.His634=
XM_011513475.1:c.1682A=	XP_011511777.1:p.His561=
XM_011513476.1:c.1901A=	XP_011511778.1:p.His634=
XM_011513477.1:c.887A=	XP_011511779.1:p.His296=
XM_011513478.1:c.611A=	XP_011511780.1:p.His204=
XR_925029.1:n.342T=
NM_001350154.1:c.845A=	NP_001337083.1:p.His282=
NM_001350155.1:c.527A=	NP_001337084.1:p.His176=
XM_011513473.3:c.1901A=	XP_011511775.1:p.His634=
XM_011513474.3:c.1901A=	XP_011511776.1:p.His634=
XM_011513475.2:c.1682A=	XP_011511777.1:p.His561=
XM_011513476.3:c.1901A=	XP_011511778.1:p.His634=
XM_011513478.2:c.611A=	XP_011511780.1:p.His204=
XM_017008284.1:c.845A=	XP_016863773.1:p.His282=
XM_017008285.1:c.845A=	XP_016863774.1:p.His282=
XM_017008286.1:c.845A=	XP_016863775.1:p.His282=
NM_001350154.2:c.845A=	NP_001337083.1:p.His282=
NM_001350155.2:c.527A=	NP_001337084.1:p.His176=
NM_000283.4:c.1682A= MANE Select	NP_000274.3:p.His561=
NM_001145291.2:c.1682A=	NP_001138763.2:p.His561=
NM_001145292.2:c.845A=	NP_001138764.2:p.His282=
NM_001350154.3:c.845A=	NP_001337083.1:p.His282=
NM_001350155.3:c.527A=	NP_001337084.1:p.His176=
NM_001379246.1:c.845A=	NP_001366175.1:p.His282=
NM_001379247.1:c.845A=	NP_001366176.1:p.His282=