Canonical Allele Identifier: CA2704991617
Gene: PDE6B HGNC NCBI

Linked Data

dbSNP Id: rs2109241905

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.660406_660407insATTCG , CM000666.2:g.660406_660407insATTCG GRCh38
NC_000004.11:g.654195_654196insATTCG , CM000666.1:g.654195_654196insATTCG GRCh37
NC_000004.10:g.644195_644196insATTCG NCBI36
NG_009839.1:g.39833_39834insATTCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000496514.6:c.1468-61_1468-60insATTCG MANE Select ENSP00000420295.1:n.1468-61_1468-60insATTCG
ENST00000255622.10:c.1468-61_1468-60insATTCG ENSP00000255622.6:n.1468-61_1468-60insATTCG
ENST00000429163.6:c.631-61_631-60insATTCG ENSP00000406334.2:n.631-61_631-60insATTCG
ENST00000496514.5:c.1468-61_1468-60insATTCG ENSP00000420295.1:n.1468-61_1468-60insATTCG
NM_000283.3:c.1468-61_1468-60insATTCG NP_000274.2:n.1468-61_1468-60insATTCG
NM_001145291.1:c.1468-61_1468-60insATTCG NP_001138763.1:n.1468-61_1468-60insATTCG
NM_001145292.1:c.631-61_631-60insATTCG NP_001138764.1:n.631-61_631-60insATTCG
XM_011513473.1:c.1687-61_1687-60insATTCG XP_011511775.1:n.1687-61_1687-60insATTCG
XM_011513474.1:c.1687-61_1687-60insATTCG XP_011511776.1:n.1687-61_1687-60insATTCG
XM_011513475.1:c.1468-61_1468-60insATTCG XP_011511777.1:n.1468-61_1468-60insATTCG
XM_011513476.1:c.1687-61_1687-60insATTCG XP_011511778.1:n.1687-61_1687-60insATTCG
XM_011513477.1:c.673-61_673-60insATTCG XP_011511779.1:n.673-61_673-60insATTCG
XM_011513478.1:c.397-61_397-60insATTCG XP_011511780.1:n.397-61_397-60insATTCG
NM_001350154.1:c.631-61_631-60insATTCG NP_001337083.1:n.631-61_631-60insATTCG
NM_001350155.1:c.313-61_313-60insATTCG NP_001337084.1:n.313-61_313-60insATTCG
XM_011513473.3:c.1687-61_1687-60insATTCG XP_011511775.1:n.1687-61_1687-60insATTCG
XM_011513474.3:c.1687-61_1687-60insATTCG XP_011511776.1:n.1687-61_1687-60insATTCG
XM_011513475.2:c.1468-61_1468-60insATTCG XP_011511777.1:n.1468-61_1468-60insATTCG
XM_011513476.3:c.1687-61_1687-60insATTCG XP_011511778.1:n.1687-61_1687-60insATTCG
XM_011513478.2:c.397-61_397-60insATTCG XP_011511780.1:n.397-61_397-60insATTCG
XM_017008284.1:c.631-61_631-60insATTCG XP_016863773.1:n.631-61_631-60insATTCG
XM_017008285.1:c.631-61_631-60insATTCG XP_016863774.1:n.631-61_631-60insATTCG
XM_017008286.1:c.631-61_631-60insATTCG XP_016863775.1:n.631-61_631-60insATTCG
NM_001350154.2:c.631-61_631-60insATTCG NP_001337083.1:n.631-61_631-60insATTCG
NM_001350155.2:c.313-61_313-60insATTCG NP_001337084.1:n.313-61_313-60insATTCG
NM_000283.4:c.1468-61_1468-60insATTCG MANE Select NP_000274.3:n.1468-61_1468-60insATTCG
NM_001145291.2:c.1468-61_1468-60insATTCG NP_001138763.2:n.1468-61_1468-60insATTCG
NM_001145292.2:c.631-61_631-60insATTCG NP_001138764.2:n.631-61_631-60insATTCG
NM_001350154.3:c.631-61_631-60insATTCG NP_001337083.1:n.631-61_631-60insATTCG
NM_001350155.3:c.313-61_313-60insATTCG NP_001337084.1:n.313-61_313-60insATTCG
NM_001379246.1:c.631-61_631-60insATTCG NP_001366175.1:n.631-61_631-60insATTCG
NM_001379247.1:c.631-61_631-60insATTCG NP_001366176.1:n.631-61_631-60insATTCG