Canonical Allele Identifier: CA388125779

Gene: CPB2 CPB2-AS1

Linked Data

• MyVariant Identifiers: chr13:g.46629899A>C (hg19) ; chr13:g.46055764A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46055764A>C , CM000675.2:g.46055764A>C	GRCh38
NC_000013.10:g.46629899A>C , CM000675.1:g.46629899A>C	GRCh37
NC_000013.9:g.45527900A>C	NCBI36
NG_032893.1:g.54313T>G
NG_032893.2:g.54270T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181383.10:c.1085T>G (CPB2) MANE Select	ENSP00000181383.4:p.Leu362Ter
ENST00000439329.5:c.974T>G (CPB2)	ENSP00000400714.3:p.Leu325Ter
ENST00000675730.1:c.*217T>G (CPB2)	ENSP00000502038.1:n.*217T>G
ENST00000181383.8:c.1085T>G (CPB2)	ENSP00000181383.4:p.Leu362Ter
ENST00000439329.4:c.974T>G (CPB2)	ENSP00000400714.3:p.Leu325Ter
NM_001278541.1:c.974T>G (CPB2)	NP_001265470.1:p.Leu325Ter
NM_001872.4:c.1085T>G (CPB2)	NP_001863.3:p.Leu362Ter
NR_046226.1:n.118+2799A>C (CPB2-AS1)
NR_046227.1:n.118+2799A>C (CPB2-AS1)
XM_017020393.2:c.1058T>G (CPB2)	XP_016875882.1:p.Leu353Ter
NM_001872.5:c.1085T>G (CPB2) MANE Select	NP_001863.3:p.Leu362Ter
NM_001278541.2:c.974T>G (CPB2)	NP_001265470.1:p.Leu325Ter