Canonical Allele Identifier: CA437901019

Gene: PDE6B

Linked Data

• dbSNP Id: rs1362087090
• gnomAD v2: 4-658688-C-A
• gnomAD v4: 4-664899-C-A
• MyVariant Identifiers: chr4:g.658688C>A (hg19) ; chr4:g.664899C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.664899C>A , CM000666.2:g.664899C>A	GRCh38
NC_000004.11:g.658688C>A , CM000666.1:g.658688C>A	GRCh37
NC_000004.10:g.648688C>A	NCBI36
NG_009839.1:g.44326C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.2148C>A MANE Select	ENSP00000420295.1:p.Ala716=
ENST00000255622.10:c.2148C>A	ENSP00000255622.6:p.Ala716=
ENST00000429163.6:c.1311C>A	ENSP00000406334.2:p.Ala437=
ENST00000460119.1:n.518C>A
ENST00000471824.6:c.228C>A	ENSP00000417852.2:p.Ala76=
ENST00000496514.5:c.2148C>A	ENSP00000420295.1:p.Ala716=
NM_000283.3:c.2148C>A	NP_000274.2:p.Ala716=
NM_001145291.1:c.2148C>A	NP_001138763.1:p.Ala716=
NM_001145292.1:c.1311C>A	NP_001138764.1:p.Ala437=
XM_011513473.1:c.2367C>A	XP_011511775.1:p.Ala789=
XM_011513474.1:c.2367C>A	XP_011511776.1:p.Ala789=
XM_011513475.1:c.2148C>A	XP_011511777.1:p.Ala716=
XM_011513476.1:c.2367C>A	XP_011511778.1:p.Ala789=
XM_011513477.1:c.1353C>A	XP_011511779.1:p.Ala451=
XM_011513478.1:c.1077C>A	XP_011511780.1:p.Ala359=
NM_001350154.1:c.1311C>A	NP_001337083.1:p.Ala437=
NM_001350155.1:c.993C>A	NP_001337084.1:p.Ala331=
XM_011513473.3:c.2367C>A	XP_011511775.1:p.Ala789=
XM_011513474.3:c.2367C>A	XP_011511776.1:p.Ala789=
XM_011513475.2:c.2148C>A	XP_011511777.1:p.Ala716=
XM_011513476.3:c.2367C>A	XP_011511778.1:p.Ala789=
XM_011513478.2:c.1077C>A	XP_011511780.1:p.Ala359=
XM_017008284.1:c.1311C>A	XP_016863773.1:p.Ala437=
XM_017008285.1:c.1311C>A	XP_016863774.1:p.Ala437=
XM_017008286.1:c.1311C>A	XP_016863775.1:p.Ala437=
NM_001350154.2:c.1311C>A	NP_001337083.1:p.Ala437=
NM_001350155.2:c.993C>A	NP_001337084.1:p.Ala331=
NM_000283.4:c.2148C>A MANE Select	NP_000274.3:p.Ala716=
NM_001145291.2:c.2148C>A	NP_001138763.2:p.Ala716=
NM_001145292.2:c.1311C>A	NP_001138764.2:p.Ala437=
NM_001350154.3:c.1311C>A	NP_001337083.1:p.Ala437=
NM_001350155.3:c.993C>A	NP_001337084.1:p.Ala331=
NM_001379246.1:c.1311C>A	NP_001366175.1:p.Ala437=
NM_001379247.1:c.1311C>A	NP_001366176.1:p.Ala437=