Canonical Allele Identifier: CA437897677

Gene: PDE6B

Linked Data

• MyVariant Identifiers: chr4:g.654282A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.660493A>T , CM000666.2:g.660493A>T	GRCh38
NC_000004.11:g.654282A>T , CM000666.1:g.654282A>T	GRCh37
NC_000004.10:g.644282A>T	NCBI36
NG_009839.1:g.39920A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496514.6:c.1494A>T MANE Select	ENSP00000420295.1:p.Thr498=
ENST00000255622.10:c.1494A>T	ENSP00000255622.6:p.Thr498=
ENST00000429163.6:c.657A>T	ENSP00000406334.2:p.Thr219=
ENST00000496514.5:c.1494A>T	ENSP00000420295.1:p.Thr498=
NM_000283.3:c.1494A>T	NP_000274.2:p.Thr498=
NM_001145291.1:c.1494A>T	NP_001138763.1:p.Thr498=
NM_001145292.1:c.657A>T	NP_001138764.1:p.Thr219=
XM_011513473.1:c.1713A>T	XP_011511775.1:p.Thr571=
XM_011513474.1:c.1713A>T	XP_011511776.1:p.Thr571=
XM_011513475.1:c.1494A>T	XP_011511777.1:p.Thr498=
XM_011513476.1:c.1713A>T	XP_011511778.1:p.Thr571=
XM_011513477.1:c.699A>T	XP_011511779.1:p.Thr233=
XM_011513478.1:c.423A>T	XP_011511780.1:p.Thr141=
NM_001350154.1:c.657A>T	NP_001337083.1:p.Thr219=
NM_001350155.1:c.339A>T	NP_001337084.1:p.Thr113=
XM_011513473.3:c.1713A>T	XP_011511775.1:p.Thr571=
XM_011513474.3:c.1713A>T	XP_011511776.1:p.Thr571=
XM_011513475.2:c.1494A>T	XP_011511777.1:p.Thr498=
XM_011513476.3:c.1713A>T	XP_011511778.1:p.Thr571=
XM_011513478.2:c.423A>T	XP_011511780.1:p.Thr141=
XM_017008284.1:c.657A>T	XP_016863773.1:p.Thr219=
XM_017008285.1:c.657A>T	XP_016863774.1:p.Thr219=
XM_017008286.1:c.657A>T	XP_016863775.1:p.Thr219=
NM_001350154.2:c.657A>T	NP_001337083.1:p.Thr219=
NM_001350155.2:c.339A>T	NP_001337084.1:p.Thr113=
NM_000283.4:c.1494A>T MANE Select	NP_000274.3:p.Thr498=
NM_001145291.2:c.1494A>T	NP_001138763.2:p.Thr498=
NM_001145292.2:c.657A>T	NP_001138764.2:p.Thr219=
NM_001350154.3:c.657A>T	NP_001337083.1:p.Thr219=
NM_001350155.3:c.339A>T	NP_001337084.1:p.Thr113=
NM_001379246.1:c.657A>T	NP_001366175.1:p.Thr219=
NM_001379247.1:c.657A>T	NP_001366176.1:p.Thr219=