Canonical Allele Identifier: CA2088943330
Gene: CPB2 HGNC NCBI
CPB2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46055793C= , CM000675.2:g.46055793C= GRCh38
NC_000013.10:g.46629928C= , CM000675.1:g.46629928C= GRCh37
NC_000013.9:g.45527929C= NCBI36
NG_032893.1:g.54284G=
NG_032893.2:g.54241G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000181383.10:c.1056G= (CPB2) MANE Select ENSP00000181383.4:p.Arg352=
ENST00000439329.5:c.945G= (CPB2) ENSP00000400714.3:p.Arg315=
ENST00000675730.1:c.*188G= (CPB2) ENSP00000502038.1:n.*188G=
ENST00000181383.8:c.1056G= (CPB2) ENSP00000181383.4:p.Arg352=
ENST00000439329.4:c.945G= (CPB2) ENSP00000400714.3:p.Arg315=
NM_001278541.1:c.945G= (CPB2) NP_001265470.1:p.Arg315=
NM_001872.4:c.1056G= (CPB2) NP_001863.3:p.Arg352=
NR_046226.1:n.118+2828C= (CPB2-AS1)
NR_046227.1:n.118+2828C= (CPB2-AS1)
XM_017020393.2:c.1029G= (CPB2) XP_016875882.1:p.Arg343=
NM_001872.5:c.1056G= (CPB2) MANE Select NP_001863.3:p.Arg352=
NM_001278541.2:c.945G= (CPB2) NP_001265470.1:p.Arg315=