Canonical Allele Identifier: CA355916899

Gene: PDE6B

Linked Data

• MyVariant Identifiers: chr4:g.655977C>G (hg19) ; chr4:g.662188C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.662188C>G , CM000666.2:g.662188C>G	GRCh38
NC_000004.11:g.655977C>G , CM000666.1:g.655977C>G	GRCh37
NC_000004.10:g.645977C>G	NCBI36
NG_009839.1:g.41615C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496514.6:c.1669C>G MANE Select	ENSP00000420295.1:p.His557Asp
ENST00000255622.10:c.1669C>G	ENSP00000255622.6:p.His557Asp
ENST00000429163.6:c.832C>G	ENSP00000406334.2:p.His278Asp
ENST00000496514.5:c.1669C>G	ENSP00000420295.1:p.His557Asp
NM_000283.3:c.1669C>G	NP_000274.2:p.His557Asp
NM_001145291.1:c.1669C>G	NP_001138763.1:p.His557Asp
NM_001145292.1:c.832C>G	NP_001138764.1:p.His278Asp
XM_011513473.1:c.1888C>G	XP_011511775.1:p.His630Asp
XM_011513474.1:c.1888C>G	XP_011511776.1:p.His630Asp
XM_011513475.1:c.1669C>G	XP_011511777.1:p.His557Asp
XM_011513476.1:c.1888C>G	XP_011511778.1:p.His630Asp
XM_011513477.1:c.874C>G	XP_011511779.1:p.His292Asp
XM_011513478.1:c.598C>G	XP_011511780.1:p.His200Asp
XR_925029.1:n.355G>C
NM_001350154.1:c.832C>G	NP_001337083.1:p.His278Asp
NM_001350155.1:c.514C>G	NP_001337084.1:p.His172Asp
XM_011513473.3:c.1888C>G	XP_011511775.1:p.His630Asp
XM_011513474.3:c.1888C>G	XP_011511776.1:p.His630Asp
XM_011513475.2:c.1669C>G	XP_011511777.1:p.His557Asp
XM_011513476.3:c.1888C>G	XP_011511778.1:p.His630Asp
XM_011513478.2:c.598C>G	XP_011511780.1:p.His200Asp
XM_017008284.1:c.832C>G	XP_016863773.1:p.His278Asp
XM_017008285.1:c.832C>G	XP_016863774.1:p.His278Asp
XM_017008286.1:c.832C>G	XP_016863775.1:p.His278Asp
NM_001350154.2:c.832C>G	NP_001337083.1:p.His278Asp
NM_001350155.2:c.514C>G	NP_001337084.1:p.His172Asp
NM_000283.4:c.1669C>G MANE Select	NP_000274.3:p.His557Asp
NM_001145291.2:c.1669C>G	NP_001138763.2:p.His557Asp
NM_001145292.2:c.832C>G	NP_001138764.2:p.His278Asp
NM_001350154.3:c.832C>G	NP_001337083.1:p.His278Asp
NM_001350155.3:c.514C>G	NP_001337084.1:p.His172Asp
NM_001379246.1:c.832C>G	NP_001366175.1:p.His278Asp
NM_001379247.1:c.832C>G	NP_001366176.1:p.His278Asp