Canonical Allele Identifier: CA2573138222

Gene: PDE6B

Linked Data

• ClinVar Variation Id: 1649835
• ClinVar RCV Id: RCV002146600
• dbSNP Id: rs934976363

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.662123G>C , CM000666.2:g.662123G>C	GRCh38
NC_000004.11:g.655912G>C , CM000666.1:g.655912G>C	GRCh37
NC_000004.10:g.645912G>C	NCBI36
NG_009839.1:g.41550G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1615-11G>C MANE Select	ENSP00000420295.1:n.1615-11G>C
ENST00000255622.10:c.1615-11G>C	ENSP00000255622.6:n.1615-11G>C
ENST00000429163.6:c.778-11G>C	ENSP00000406334.2:n.778-11G>C
ENST00000496514.5:c.1615-11G>C	ENSP00000420295.1:n.1615-11G>C
NM_000283.3:c.1615-11G>C	NP_000274.2:n.1615-11G>C
NM_001145291.1:c.1615-11G>C	NP_001138763.1:n.1615-11G>C
NM_001145292.1:c.778-11G>C	NP_001138764.1:n.778-11G>C
XM_011513473.1:c.1834-11G>C	XP_011511775.1:n.1834-11G>C
XM_011513474.1:c.1834-11G>C	XP_011511776.1:n.1834-11G>C
XM_011513475.1:c.1615-11G>C	XP_011511777.1:n.1615-11G>C
XM_011513476.1:c.1834-11G>C	XP_011511778.1:n.1834-11G>C
XM_011513477.1:c.820-11G>C	XP_011511779.1:n.820-11G>C
XM_011513478.1:c.544-11G>C	XP_011511780.1:n.544-11G>C
XR_925029.1:n.420C>G
NM_001350154.1:c.778-11G>C	NP_001337083.1:n.778-11G>C
NM_001350155.1:c.460-11G>C	NP_001337084.1:n.460-11G>C
XM_011513473.3:c.1834-11G>C	XP_011511775.1:n.1834-11G>C
XM_011513474.3:c.1834-11G>C	XP_011511776.1:n.1834-11G>C
XM_011513475.2:c.1615-11G>C	XP_011511777.1:n.1615-11G>C
XM_011513476.3:c.1834-11G>C	XP_011511778.1:n.1834-11G>C
XM_011513478.2:c.544-11G>C	XP_011511780.1:n.544-11G>C
XM_017008284.1:c.778-11G>C	XP_016863773.1:n.778-11G>C
XM_017008285.1:c.778-11G>C	XP_016863774.1:n.778-11G>C
XM_017008286.1:c.778-11G>C	XP_016863775.1:n.778-11G>C
NM_001350154.2:c.778-11G>C	NP_001337083.1:n.778-11G>C
NM_001350155.2:c.460-11G>C	NP_001337084.1:n.460-11G>C
NM_000283.4:c.1615-11G>C MANE Select	NP_000274.3:n.1615-11G>C
NM_001145291.2:c.1615-11G>C	NP_001138763.2:n.1615-11G>C
NM_001145292.2:c.778-11G>C	NP_001138764.2:n.778-11G>C
NM_001350154.3:c.778-11G>C	NP_001337083.1:n.778-11G>C
NM_001350155.3:c.460-11G>C	NP_001337084.1:n.460-11G>C
NM_001379246.1:c.778-11G>C	NP_001366175.1:n.778-11G>C
NM_001379247.1:c.778-11G>C	NP_001366176.1:n.778-11G>C