Canonical Allele Identifier: CA355915799

Gene: PDE6B

Linked Data

• gnomAD v4: 4-660491-A-G
• MyVariant Identifiers: chr4:g.654280A>G (hg19) ; chr4:g.660491A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.660491A>G , CM000666.2:g.660491A>G	GRCh38
NC_000004.11:g.654280A>G , CM000666.1:g.654280A>G	GRCh37
NC_000004.10:g.644280A>G	NCBI36
NG_009839.1:g.39918A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1492A>G MANE Select	ENSP00000420295.1:p.Thr498Ala
ENST00000255622.10:c.1492A>G	ENSP00000255622.6:p.Thr498Ala
ENST00000429163.6:c.655A>G	ENSP00000406334.2:p.Thr219Ala
ENST00000496514.5:c.1492A>G	ENSP00000420295.1:p.Thr498Ala
NM_000283.3:c.1492A>G	NP_000274.2:p.Thr498Ala
NM_001145291.1:c.1492A>G	NP_001138763.1:p.Thr498Ala
NM_001145292.1:c.655A>G	NP_001138764.1:p.Thr219Ala
XM_011513473.1:c.1711A>G	XP_011511775.1:p.Thr571Ala
XM_011513474.1:c.1711A>G	XP_011511776.1:p.Thr571Ala
XM_011513475.1:c.1492A>G	XP_011511777.1:p.Thr498Ala
XM_011513476.1:c.1711A>G	XP_011511778.1:p.Thr571Ala
XM_011513477.1:c.697A>G	XP_011511779.1:p.Thr233Ala
XM_011513478.1:c.421A>G	XP_011511780.1:p.Thr141Ala
NM_001350154.1:c.655A>G	NP_001337083.1:p.Thr219Ala
NM_001350155.1:c.337A>G	NP_001337084.1:p.Thr113Ala
XM_011513473.3:c.1711A>G	XP_011511775.1:p.Thr571Ala
XM_011513474.3:c.1711A>G	XP_011511776.1:p.Thr571Ala
XM_011513475.2:c.1492A>G	XP_011511777.1:p.Thr498Ala
XM_011513476.3:c.1711A>G	XP_011511778.1:p.Thr571Ala
XM_011513478.2:c.421A>G	XP_011511780.1:p.Thr141Ala
XM_017008284.1:c.655A>G	XP_016863773.1:p.Thr219Ala
XM_017008285.1:c.655A>G	XP_016863774.1:p.Thr219Ala
XM_017008286.1:c.655A>G	XP_016863775.1:p.Thr219Ala
NM_001350154.2:c.655A>G	NP_001337083.1:p.Thr219Ala
NM_001350155.2:c.337A>G	NP_001337084.1:p.Thr113Ala
NM_000283.4:c.1492A>G MANE Select	NP_000274.3:p.Thr498Ala
NM_001145291.2:c.1492A>G	NP_001138763.2:p.Thr498Ala
NM_001145292.2:c.655A>G	NP_001138764.2:p.Thr219Ala
NM_001350154.3:c.655A>G	NP_001337083.1:p.Thr219Ala
NM_001350155.3:c.337A>G	NP_001337084.1:p.Thr113Ala
NM_001379246.1:c.655A>G	NP_001366175.1:p.Thr219Ala
NM_001379247.1:c.655A>G	NP_001366176.1:p.Thr219Ala