Canonical Allele Identifier: CA438053440

Gene: PDE6B

Linked Data

• dbSNP Id: rs1205125431
• gnomAD v2: 4-655937-C-T
• gnomAD v4: 4-662148-C-T
• MyVariant Identifiers: chr4:g.655937C>T (hg19) ; chr4:g.662148C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.662148C>T , CM000666.2:g.662148C>T	GRCh38
NC_000004.11:g.655937C>T , CM000666.1:g.655937C>T	GRCh37
NC_000004.10:g.645937C>T	NCBI36
NG_009839.1:g.41575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1629C>T MANE Select	ENSP00000420295.1:p.Phe543=
ENST00000255622.10:c.1629C>T	ENSP00000255622.6:p.Phe543=
ENST00000429163.6:c.792C>T	ENSP00000406334.2:p.Phe264=
ENST00000496514.5:c.1629C>T	ENSP00000420295.1:p.Phe543=
NM_000283.3:c.1629C>T	NP_000274.2:p.Phe543=
NM_001145291.1:c.1629C>T	NP_001138763.1:p.Phe543=
NM_001145292.1:c.792C>T	NP_001138764.1:p.Phe264=
XM_011513473.1:c.1848C>T	XP_011511775.1:p.Phe616=
XM_011513474.1:c.1848C>T	XP_011511776.1:p.Phe616=
XM_011513475.1:c.1629C>T	XP_011511777.1:p.Phe543=
XM_011513476.1:c.1848C>T	XP_011511778.1:p.Phe616=
XM_011513477.1:c.834C>T	XP_011511779.1:p.Phe278=
XM_011513478.1:c.558C>T	XP_011511780.1:p.Phe186=
XR_925029.1:n.395G>A
NM_001350154.1:c.792C>T	NP_001337083.1:p.Phe264=
NM_001350155.1:c.474C>T	NP_001337084.1:p.Phe158=
XM_011513473.3:c.1848C>T	XP_011511775.1:p.Phe616=
XM_011513474.3:c.1848C>T	XP_011511776.1:p.Phe616=
XM_011513475.2:c.1629C>T	XP_011511777.1:p.Phe543=
XM_011513476.3:c.1848C>T	XP_011511778.1:p.Phe616=
XM_011513478.2:c.558C>T	XP_011511780.1:p.Phe186=
XM_017008284.1:c.792C>T	XP_016863773.1:p.Phe264=
XM_017008285.1:c.792C>T	XP_016863774.1:p.Phe264=
XM_017008286.1:c.792C>T	XP_016863775.1:p.Phe264=
NM_001350154.2:c.792C>T	NP_001337083.1:p.Phe264=
NM_001350155.2:c.474C>T	NP_001337084.1:p.Phe158=
NM_000283.4:c.1629C>T MANE Select	NP_000274.3:p.Phe543=
NM_001145291.2:c.1629C>T	NP_001138763.2:p.Phe543=
NM_001145292.2:c.792C>T	NP_001138764.2:p.Phe264=
NM_001350154.3:c.792C>T	NP_001337083.1:p.Phe264=
NM_001350155.3:c.474C>T	NP_001337084.1:p.Phe158=
NM_001379246.1:c.792C>T	NP_001366175.1:p.Phe264=
NM_001379247.1:c.792C>T	NP_001366176.1:p.Phe264=