Canonical Allele Identifier: CA7700563
Gene: AP3B2 HGNC NCBI
CPEB1-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374850
ClinVar RCV Id: RCV000415580
dbSNP Id: rs775024756

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.82689223G>A , CM000677.2:g.82689223G>A GRCh38
NC_000015.9:g.83357975G>A , CM000677.1:g.83357975G>A GRCh37
NC_000015.8:g.81155029G>A NCBI36
NG_052957.1:g.25686C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261722.8:c.199C>T ENSP00000261722.4:p.Arg67Ter
ENST00000535359.6:c.199C>T MANE Select ENSP00000440984.1:p.Arg67Ter
ENST00000535385.6:n.376C>T
ENST00000535513.2:c.199C>T ENSP00000499258.1:p.Arg67Ter
ENST00000537735.2:n.345C>T
ENST00000543938.6:n.402C>T
ENST00000642989.2:c.328C>T ENSP00000493485.1:p.Arg110Ter
ENST00000652847.1:c.199C>T ENSP00000499785.1:p.Arg67Ter
ENST00000657321.1:c.199C>T ENSP00000499716.1:p.Arg67Ter
ENST00000663651.1:n.341C>T
ENST00000664460.1:c.199C>T ENSP00000499798.1:p.Arg67Ter
ENST00000666055.1:c.199C>T ENSP00000499608.1:p.Arg67Ter
ENST00000666973.1:c.199C>T ENSP00000499288.1:p.Arg67Ter
ENST00000667758.1:c.199C>T ENSP00000499318.1:p.Arg67Ter
ENST00000668385.1:c.190-111C>T ENSP00000499544.1:p.=
ENST00000668990.2:c.199C>T ENSP00000499235.1:p.Arg67Ter
ENST00000669930.1:c.189+155C>T ENSP00000499671.1:p.=
ENST00000679388.1:n.138C>T
ENST00000679531.1:n.605C>T
ENST00000679950.1:n.408C>T
ENST00000680492.1:n.605C>T
ENST00000680946.1:n.605C>T
ENST00000681044.1:n.605C>T
ENST00000681327.1:c.199C>T ENSP00000505423.1:p.Arg67Ter
ENST00000681452.1:n.605C>T
ENST00000681464.1:n.605C>T
ENST00000261722.7:c.199C>T ENSP00000261722.3:p.Arg67Ter
ENST00000535348.5:c.199C>T ENSP00000438721.1:p.Arg67Ter
ENST00000535359.5:c.199C>T ENSP00000440984.1:p.Arg67Ter
ENST00000535385.5:n.376C>T
ENST00000535513.1:n.366C>T
ENST00000541693.5:c.67C>T ENSP00000441961.1:p.Arg23Ter
ENST00000542200.2:c.199C>T ENSP00000440719.1:p.Arg67Ter
ENST00000561455.5:n.166C>T
ENST00000620652.4:c.199C>T ENSP00000479229.1:p.Arg67Ter
NM_001278511.1:c.199C>T (AP3B2) NP_001265440.1:p.Arg67Ter
NM_001278512.1:c.199C>T (AP3B2) NP_001265441.1:p.Arg67Ter
NM_004644.4:c.199C>T (AP3B2) NP_004635.2:p.Arg67Ter
NR_046096.1:n.1329-2788G>A (CPEB1-AS1)
XM_011522097.1:c.199C>T (AP3B2) XP_011520399.1:p.Arg67Ter
XM_011522098.1:c.199C>T (AP3B2) XP_011520400.1:p.Arg67Ter
XM_011522099.1:c.199C>T (AP3B2) XP_011520401.1:p.Arg67Ter
NM_001348440.1:c.199C>T (AP3B2) NP_001335369.1:p.Arg67Ter
XM_017022640.2:c.199C>T (AP3B2) XP_016878129.1:p.Arg67Ter
XM_017022641.2:c.199C>T (AP3B2) XP_016878130.1:p.Arg67Ter
XR_001751404.2:n.365C>T (AP3B2)
NM_001278512.2:c.199C>T (AP3B2) MANE Select NP_001265441.1:p.Arg67Ter
NM_004644.5:c.199C>T (AP3B2) NP_004635.2:p.Arg67Ter
NM_001278511.2:c.199C>T (AP3B2) NP_001265440.1:p.Arg67Ter
NM_001348440.2:c.199C>T (AP3B2) NP_001335369.1:p.Arg67Ter