Canonical Allele Identifier: CA2630003700

Gene: AP3B2 CPEB1-AS1

Linked Data

• gnomAD v4: 15-82689030-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82689030T>C , CM000677.2:g.82689030T>C	GRCh38
NC_000015.9:g.83357782T>C , CM000677.1:g.83357782T>C	GRCh37
NC_000015.8:g.81154836T>C	NCBI36
NG_052957.1:g.25879A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261722.8:c.264+128A>G (AP3B2)	ENSP00000261722.4:n.264+128A>G
ENST00000535359.6:c.264+128A>G (AP3B2) MANE Select	ENSP00000440984.1:n.264+128A>G
ENST00000535385.6:n.569A>G (AP3B2)
ENST00000535513.2:c.264+128A>G (AP3B2)	ENSP00000499258.1:n.264+128A>G
ENST00000537735.2:n.410+128A>G (AP3B2)
ENST00000543938.6:n.467+128A>G (AP3B2)
ENST00000642989.2:c.393+128A>G (AP3B2)	ENSP00000493485.1:n.393+128A>G
ENST00000652847.1:c.264+128A>G (AP3B2)	ENSP00000499785.1:n.264+128A>G
ENST00000657321.1:c.264+128A>G (AP3B2)	ENSP00000499716.1:n.264+128A>G
ENST00000663651.1:n.406+128A>G (AP3B2)
ENST00000664460.1:c.264+128A>G (AP3B2)	ENSP00000499798.1:n.264+128A>G
ENST00000666055.1:c.264+128A>G (AP3B2)	ENSP00000499608.1:n.264+128A>G
ENST00000666973.1:c.264+128A>G (AP3B2)	ENSP00000499288.1:n.264+128A>G
ENST00000667758.1:c.*110A>G (AP3B2)	ENSP00000499318.1:n.*110A>G
ENST00000668385.1:c.*20A>G (AP3B2)	ENSP00000499544.1:n.*20A>G
ENST00000668990.2:c.264+128A>G (AP3B2)	ENSP00000499235.1:n.264+128A>G
ENST00000669930.1:c.189+348A>G (AP3B2)	ENSP00000499671.1:n.189+348A>G
ENST00000679388.1:n.203+128A>G (AP3B2)
ENST00000679531.1:n.670+128A>G (AP3B2)
ENST00000679950.1:n.601A>G (AP3B2)
ENST00000680492.1:n.670+128A>G (AP3B2)
ENST00000680946.1:n.670+128A>G (AP3B2)
ENST00000681044.1:n.670+128A>G (AP3B2)
ENST00000681327.1:c.264+128A>G (AP3B2)	ENSP00000505423.1:n.264+128A>G
ENST00000681452.1:n.670+128A>G (AP3B2)
ENST00000681464.1:n.670+128A>G (AP3B2)
ENST00000261722.7:c.264+128A>G (AP3B2)	ENSP00000261722.3:n.264+128A>G
ENST00000535348.5:c.264+128A>G (AP3B2)	ENSP00000438721.1:n.264+128A>G
ENST00000535359.5:c.264+128A>G (AP3B2)	ENSP00000440984.1:n.264+128A>G
ENST00000535385.5:n.569A>G (AP3B2)
ENST00000535513.1:n.431+128A>G (AP3B2)
ENST00000541693.5:c.132+128A>G (AP3B2)	ENSP00000441961.1:n.132+128A>G
ENST00000542200.2:c.264+128A>G (AP3B2)	ENSP00000440719.1:n.264+128A>G
ENST00000561455.5:n.231+128A>G (AP3B2)
ENST00000620652.4:c.264+128A>G (AP3B2)	ENSP00000479229.1:n.264+128A>G
NM_001278511.1:c.264+128A>G (AP3B2)	NP_001265440.1:n.264+128A>G
NM_001278512.1:c.264+128A>G (AP3B2)	NP_001265441.1:n.264+128A>G
NM_004644.4:c.264+128A>G (AP3B2)	NP_004635.2:n.264+128A>G
NR_046096.1:n.1329-2981T>C (CPEB1-AS1)
XM_011522097.1:c.264+128A>G (AP3B2)	XP_011520399.1:n.264+128A>G
XM_011522098.1:c.264+128A>G (AP3B2)	XP_011520400.1:n.264+128A>G
XM_011522099.1:c.264+128A>G (AP3B2)	XP_011520401.1:n.264+128A>G
NM_001348440.1:c.264+128A>G (AP3B2)	NP_001335369.1:n.264+128A>G
XM_017022640.2:c.264+128A>G (AP3B2)	XP_016878129.1:n.264+128A>G
XM_017022641.2:c.264+128A>G (AP3B2)	XP_016878130.1:n.264+128A>G
XR_001751404.2:n.430+128A>G (AP3B2)
NM_001278512.2:c.264+128A>G (AP3B2) MANE Select	NP_001265441.1:n.264+128A>G
NM_004644.5:c.264+128A>G (AP3B2)	NP_004635.2:n.264+128A>G
NM_001278511.2:c.264+128A>G (AP3B2)	NP_001265440.1:n.264+128A>G
NM_001348440.2:c.264+128A>G (AP3B2)	NP_001335369.1:n.264+128A>G