Canonical Allele Identifier: CA355919712
Gene: PDE6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.664919C>A , CM000666.2:g.664919C>A GRCh38
NC_000004.11:g.658708C>A , CM000666.1:g.658708C>A GRCh37
NC_000004.10:g.648708C>A NCBI36
NG_009839.1:g.44346C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496514.6:c.2168C>A MANE Select ENSP00000420295.1:p.Thr723Asn
ENST00000255622.10:c.2168C>A ENSP00000255622.6:p.Thr723Asn
ENST00000429163.6:c.1331C>A ENSP00000406334.2:p.Thr444Asn
ENST00000460119.1:n.538C>A
ENST00000461490.1:c.10C>A
ENST00000471824.6:c.248C>A ENSP00000417852.2:p.Thr83Asn
ENST00000496514.5:c.2168C>A ENSP00000420295.1:p.Thr723Asn
NM_000283.3:c.2168C>A NP_000274.2:p.Thr723Asn
NM_001145291.1:c.2168C>A NP_001138763.1:p.Thr723Asn
NM_001145292.1:c.1331C>A NP_001138764.1:p.Thr444Asn
XM_011513473.1:c.2387C>A XP_011511775.1:p.Thr796Asn
XM_011513474.1:c.2387C>A XP_011511776.1:p.Thr796Asn
XM_011513475.1:c.2168C>A XP_011511777.1:p.Thr723Asn
XM_011513476.1:c.2387C>A XP_011511778.1:p.Thr796Asn
XM_011513477.1:c.1373C>A XP_011511779.1:p.Thr458Asn
XM_011513478.1:c.1097C>A XP_011511780.1:p.Thr366Asn
NM_001350154.1:c.1331C>A NP_001337083.1:p.Thr444Asn
NM_001350155.1:c.1013C>A NP_001337084.1:p.Thr338Asn
XM_011513473.3:c.2387C>A XP_011511775.1:p.Thr796Asn
XM_011513474.3:c.2387C>A XP_011511776.1:p.Thr796Asn
XM_011513475.2:c.2168C>A XP_011511777.1:p.Thr723Asn
XM_011513476.3:c.2387C>A XP_011511778.1:p.Thr796Asn
XM_011513478.2:c.1097C>A XP_011511780.1:p.Thr366Asn
XM_017008284.1:c.1331C>A XP_016863773.1:p.Thr444Asn
XM_017008285.1:c.1331C>A XP_016863774.1:p.Thr444Asn
XM_017008286.1:c.1331C>A XP_016863775.1:p.Thr444Asn
NM_001350154.2:c.1331C>A NP_001337083.1:p.Thr444Asn
NM_001350155.2:c.1013C>A NP_001337084.1:p.Thr338Asn
NM_000283.4:c.2168C>A MANE Select NP_000274.3:p.Thr723Asn
NM_001145291.2:c.2168C>A NP_001138763.2:p.Thr723Asn
NM_001145292.2:c.1331C>A NP_001138764.2:p.Thr444Asn
NM_001350154.3:c.1331C>A NP_001337083.1:p.Thr444Asn
NM_001350155.3:c.1013C>A NP_001337084.1:p.Thr338Asn
NM_001379246.1:c.1331C>A NP_001366175.1:p.Thr444Asn
NM_001379247.1:c.1331C>A NP_001366176.1:p.Thr444Asn