Canonical Allele Identifier: CA2795039

Gene: PDE6B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.667866G>A , CM000666.2:g.667866G>A	GRCh38
NC_000004.11:g.661655G>A , CM000666.1:g.661655G>A	GRCh37
NC_000004.10:g.651655G>A	NCBI36
NG_009839.1:g.47293G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.2363G>A MANE Select	ENSP00000420295.1:p.Arg788His
ENST00000255622.10:c.2363G>A	ENSP00000255622.6:p.Arg788His
ENST00000429163.6:c.1526G>A	ENSP00000406334.2:p.Arg509His
ENST00000461490.1:c.205G>A
ENST00000471824.6:c.432+1252G>A	ENSP00000417852.2:n.432+1252G>A
ENST00000496514.5:c.2363G>A	ENSP00000420295.1:p.Arg788His
NM_000283.3:c.2363G>A	NP_000274.2:p.Arg788His
NM_001145291.1:c.2363G>A	NP_001138763.1:p.Arg788His
NM_001145292.1:c.1526G>A	NP_001138764.1:p.Arg509His
XM_011513473.1:c.2582G>A	XP_011511775.1:p.Arg861His
XM_011513474.1:c.2582G>A	XP_011511776.1:p.Arg861His
XM_011513475.1:c.2363G>A	XP_011511777.1:p.Arg788His
XM_011513476.1:c.2571+1252G>A	XP_011511778.1:n.2571+1252G>A
XM_011513477.1:c.1568G>A	XP_011511779.1:p.Arg523His
XM_011513478.1:c.1292G>A	XP_011511780.1:p.Arg431His
NM_001350154.1:c.1526G>A	NP_001337083.1:p.Arg509His
NM_001350155.1:c.1208G>A	NP_001337084.1:p.Arg403His
XM_011513473.3:c.2582G>A	XP_011511775.1:p.Arg861His
XM_011513474.3:c.2582G>A	XP_011511776.1:p.Arg861His
XM_011513475.2:c.2363G>A	XP_011511777.1:p.Arg788His
XM_011513476.3:c.2571+1252G>A	XP_011511778.1:n.2571+1252G>A
XM_011513478.2:c.1292G>A	XP_011511780.1:p.Arg431His
XM_017008284.1:c.1526G>A	XP_016863773.1:p.Arg509His
XM_017008285.1:c.1526G>A	XP_016863774.1:p.Arg509His
XM_017008286.1:c.1526G>A	XP_016863775.1:p.Arg509His
NM_001350154.2:c.1526G>A	NP_001337083.1:p.Arg509His
NM_001350155.2:c.1208G>A	NP_001337084.1:p.Arg403His
NM_000283.4:c.2363G>A MANE Select	NP_000274.3:p.Arg788His
NM_001145291.2:c.2363G>A	NP_001138763.2:p.Arg788His
NM_001145292.2:c.1526G>A	NP_001138764.2:p.Arg509His
NM_001350154.3:c.1526G>A	NP_001337083.1:p.Arg509His
NM_001350155.3:c.1208G>A	NP_001337084.1:p.Arg403His
NM_001379246.1:c.1526G>A	NP_001366175.1:p.Arg509His
NM_001379247.1:c.1526G>A	NP_001366176.1:p.Arg509His