Canonical Allele Identifier: CA2575409759

Gene: CPB2 CPB2-AS1

Linked Data

• gnomAD v4: 13-46055720-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46055720A>T , CM000675.2:g.46055720A>T	GRCh38
NC_000013.10:g.46629855A>T , CM000675.1:g.46629855A>T	GRCh37
NC_000013.9:g.45527856A>T	NCBI36
NG_032893.1:g.54357T>A
NG_032893.2:g.54314T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181383.10:c.1087+42T>A (CPB2) MANE Select	ENSP00000181383.4:n.1087+42T>A
ENST00000439329.5:c.976+42T>A (CPB2)	ENSP00000400714.3:n.976+42T>A
ENST00000675730.1:c.*219+42T>A (CPB2)	ENSP00000502038.1:n.*219+42T>A
ENST00000181383.8:c.1087+42T>A (CPB2)	ENSP00000181383.4:n.1087+42T>A
ENST00000439329.4:c.976+42T>A (CPB2)	ENSP00000400714.3:n.976+42T>A
NM_001278541.1:c.976+42T>A (CPB2)	NP_001265470.1:n.976+42T>A
NM_001872.4:c.1087+42T>A (CPB2)	NP_001863.3:n.1087+42T>A
NR_046226.1:n.118+2755A>T (CPB2-AS1)
NR_046227.1:n.118+2755A>T (CPB2-AS1)
XM_017020393.2:c.1060+42T>A (CPB2)	XP_016875882.1:n.1060+42T>A
NM_001872.5:c.1087+42T>A (CPB2) MANE Select	NP_001863.3:n.1087+42T>A
NM_001278541.2:c.976+42T>A (CPB2)	NP_001265470.1:n.976+42T>A