Canonical Allele Identifier: CA355919738
Gene: PDE6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.664924C>T , CM000666.2:g.664924C>T GRCh38
NC_000004.11:g.658713C>T , CM000666.1:g.658713C>T GRCh37
NC_000004.10:g.648713C>T NCBI36
NG_009839.1:g.44351C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496514.6:c.2173C>T MANE Select ENSP00000420295.1:p.Pro725Ser
ENST00000255622.10:c.2173C>T ENSP00000255622.6:p.Pro725Ser
ENST00000429163.6:c.1336C>T ENSP00000406334.2:p.Pro446Ser
ENST00000461490.1:c.15C>T
ENST00000471824.6:c.253C>T ENSP00000417852.2:p.Pro85Ser
ENST00000496514.5:c.2173C>T ENSP00000420295.1:p.Pro725Ser
NM_000283.3:c.2173C>T NP_000274.2:p.Pro725Ser
NM_001145291.1:c.2173C>T NP_001138763.1:p.Pro725Ser
NM_001145292.1:c.1336C>T NP_001138764.1:p.Pro446Ser
XM_011513473.1:c.2392C>T XP_011511775.1:p.Pro798Ser
XM_011513474.1:c.2392C>T XP_011511776.1:p.Pro798Ser
XM_011513475.1:c.2173C>T XP_011511777.1:p.Pro725Ser
XM_011513476.1:c.2392C>T XP_011511778.1:p.Pro798Ser
XM_011513477.1:c.1378C>T XP_011511779.1:p.Pro460Ser
XM_011513478.1:c.1102C>T XP_011511780.1:p.Pro368Ser
NM_001350154.1:c.1336C>T NP_001337083.1:p.Pro446Ser
NM_001350155.1:c.1018C>T NP_001337084.1:p.Pro340Ser
XM_011513473.3:c.2392C>T XP_011511775.1:p.Pro798Ser
XM_011513474.3:c.2392C>T XP_011511776.1:p.Pro798Ser
XM_011513475.2:c.2173C>T XP_011511777.1:p.Pro725Ser
XM_011513476.3:c.2392C>T XP_011511778.1:p.Pro798Ser
XM_011513478.2:c.1102C>T XP_011511780.1:p.Pro368Ser
XM_017008284.1:c.1336C>T XP_016863773.1:p.Pro446Ser
XM_017008285.1:c.1336C>T XP_016863774.1:p.Pro446Ser
XM_017008286.1:c.1336C>T XP_016863775.1:p.Pro446Ser
NM_001350154.2:c.1336C>T NP_001337083.1:p.Pro446Ser
NM_001350155.2:c.1018C>T NP_001337084.1:p.Pro340Ser
NM_000283.4:c.2173C>T MANE Select NP_000274.3:p.Pro725Ser
NM_001145291.2:c.2173C>T NP_001138763.2:p.Pro725Ser
NM_001145292.2:c.1336C>T NP_001138764.2:p.Pro446Ser
NM_001350154.3:c.1336C>T NP_001337083.1:p.Pro446Ser
NM_001350155.3:c.1018C>T NP_001337084.1:p.Pro340Ser
NM_001379246.1:c.1336C>T NP_001366175.1:p.Pro446Ser
NM_001379247.1:c.1336C>T NP_001366176.1:p.Pro446Ser