Canonical Allele Identifier: CA437897767

Gene: PDE6B

Linked Data

• MyVariant Identifiers: chr4:g.654379C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.660590C>A , CM000666.2:g.660590C>A	GRCh38
NC_000004.11:g.654379C>A , CM000666.1:g.654379C>A	GRCh37
NC_000004.10:g.644379C>A	NCBI36
NG_009839.1:g.40017C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1591C>A MANE Select	ENSP00000420295.1:p.Arg531=
ENST00000255622.10:c.1591C>A	ENSP00000255622.6:p.Arg531=
ENST00000429163.6:c.754C>A	ENSP00000406334.2:p.Arg252=
ENST00000496514.5:c.1591C>A	ENSP00000420295.1:p.Arg531=
NM_000283.3:c.1591C>A	NP_000274.2:p.Arg531=
NM_001145291.1:c.1591C>A	NP_001138763.1:p.Arg531=
NM_001145292.1:c.754C>A	NP_001138764.1:p.Arg252=
XM_011513473.1:c.1810C>A	XP_011511775.1:p.Arg604=
XM_011513474.1:c.1810C>A	XP_011511776.1:p.Arg604=
XM_011513475.1:c.1591C>A	XP_011511777.1:p.Arg531=
XM_011513476.1:c.1810C>A	XP_011511778.1:p.Arg604=
XM_011513477.1:c.796C>A	XP_011511779.1:p.Arg266=
XM_011513478.1:c.520C>A	XP_011511780.1:p.Arg174=
NM_001350154.1:c.754C>A	NP_001337083.1:p.Arg252=
NM_001350155.1:c.436C>A	NP_001337084.1:p.Arg146=
XM_011513473.3:c.1810C>A	XP_011511775.1:p.Arg604=
XM_011513474.3:c.1810C>A	XP_011511776.1:p.Arg604=
XM_011513475.2:c.1591C>A	XP_011511777.1:p.Arg531=
XM_011513476.3:c.1810C>A	XP_011511778.1:p.Arg604=
XM_011513478.2:c.520C>A	XP_011511780.1:p.Arg174=
XM_017008284.1:c.754C>A	XP_016863773.1:p.Arg252=
XM_017008285.1:c.754C>A	XP_016863774.1:p.Arg252=
XM_017008286.1:c.754C>A	XP_016863775.1:p.Arg252=
NM_001350154.2:c.754C>A	NP_001337083.1:p.Arg252=
NM_001350155.2:c.436C>A	NP_001337084.1:p.Arg146=
NM_000283.4:c.1591C>A MANE Select	NP_000274.3:p.Arg531=
NM_001145291.2:c.1591C>A	NP_001138763.2:p.Arg531=
NM_001145292.2:c.754C>A	NP_001138764.2:p.Arg252=
NM_001350154.3:c.754C>A	NP_001337083.1:p.Arg252=
NM_001350155.3:c.436C>A	NP_001337084.1:p.Arg146=
NM_001379246.1:c.754C>A	NP_001366175.1:p.Arg252=
NM_001379247.1:c.754C>A	NP_001366176.1:p.Arg252=