Canonical Allele Identifier: CA2794631

Gene: PDE6B

Linked Data

• ClinVar Variation Id: 942252
• ClinVar RCV Id: RCV001212202
• dbSNP Id: rs777799273
• ExAC: 4:655987 G / A
• gnomAD v2: 4-655987-G-A
• gnomAD v3: 4-662198-G-A
• gnomAD v4: 4-662198-G-A
• MyVariant Identifiers: chr4:g.655987G>A (hg19) ; chr4:g.662198G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.662198G>A , CM000666.2:g.662198G>A	GRCh38
NC_000004.11:g.655987G>A , CM000666.1:g.655987G>A	GRCh37
NC_000004.10:g.645987G>A	NCBI36
NG_009839.1:g.41625G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1679G>A MANE Select	ENSP00000420295.1:p.Arg560His
ENST00000255622.10:c.1679G>A	ENSP00000255622.6:p.Arg560His
ENST00000429163.6:c.842G>A	ENSP00000406334.2:p.Arg281His
ENST00000496514.5:c.1679G>A	ENSP00000420295.1:p.Arg560His
NM_000283.3:c.1679G>A	NP_000274.2:p.Arg560His
NM_001145291.1:c.1679G>A	NP_001138763.1:p.Arg560His
NM_001145292.1:c.842G>A	NP_001138764.1:p.Arg281His
XM_011513473.1:c.1898G>A	XP_011511775.1:p.Arg633His
XM_011513474.1:c.1898G>A	XP_011511776.1:p.Arg633His
XM_011513475.1:c.1679G>A	XP_011511777.1:p.Arg560His
XM_011513476.1:c.1898G>A	XP_011511778.1:p.Arg633His
XM_011513477.1:c.884G>A	XP_011511779.1:p.Arg295His
XM_011513478.1:c.608G>A	XP_011511780.1:p.Arg203His
XR_925029.1:n.345C>T
NM_001350154.1:c.842G>A	NP_001337083.1:p.Arg281His
NM_001350155.1:c.524G>A	NP_001337084.1:p.Arg175His
XM_011513473.3:c.1898G>A	XP_011511775.1:p.Arg633His
XM_011513474.3:c.1898G>A	XP_011511776.1:p.Arg633His
XM_011513475.2:c.1679G>A	XP_011511777.1:p.Arg560His
XM_011513476.3:c.1898G>A	XP_011511778.1:p.Arg633His
XM_011513478.2:c.608G>A	XP_011511780.1:p.Arg203His
XM_017008284.1:c.842G>A	XP_016863773.1:p.Arg281His
XM_017008285.1:c.842G>A	XP_016863774.1:p.Arg281His
XM_017008286.1:c.842G>A	XP_016863775.1:p.Arg281His
NM_001350154.2:c.842G>A	NP_001337083.1:p.Arg281His
NM_001350155.2:c.524G>A	NP_001337084.1:p.Arg175His
NM_000283.4:c.1679G>A MANE Select	NP_000274.3:p.Arg560His
NM_001145291.2:c.1679G>A	NP_001138763.2:p.Arg560His
NM_001145292.2:c.842G>A	NP_001138764.2:p.Arg281His
NM_001350154.3:c.842G>A	NP_001337083.1:p.Arg281His
NM_001350155.3:c.524G>A	NP_001337084.1:p.Arg175His
NM_001379246.1:c.842G>A	NP_001366175.1:p.Arg281His
NM_001379247.1:c.842G>A	NP_001366176.1:p.Arg281His