Canonical Allele Identifier: CA1619255816

Gene: CSNK2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31667936A= , CM000668.2:g.31667936A=	GRCh38
NC_000006.11:g.31635713A= , CM000668.1:g.31635713A=	GRCh37
NC_000006.10:g.31743692A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375882.7:c.141A= MANE Select	ENSP00000365042.3:p.Arg47=
ENST00000465481.6:n.274A=
ENST00000475875.2:n.1224A=
ENST00000677388.1:c.198A=	ENSP00000504290.1:p.Arg66=
ENST00000677536.1:c.198A=	ENSP00000502967.1:p.Arg66=
ENST00000677758.1:c.198A=	ENSP00000504242.1:p.Arg66=
ENST00000375865.6:c.141A=	ENSP00000365025.2:p.Arg47=
ENST00000375866.2:c.141A=	ENSP00000365026.2:p.Arg47=
ENST00000375880.6:c.141A=	ENSP00000365040.2:p.Arg47=
ENST00000375882.6:c.141A=	ENSP00000365042.2:p.Arg47=
ENST00000375885.8:c.198A=	ENSP00000365046.4:p.Arg66=
ENST00000465481.5:n.274A=
ENST00000468255.5:n.280A=
ENST00000481269.1:n.267A=
ENST00000617558.2:c.141A=	ENSP00000483989.2:p.Arg47=
NM_001282385.1:c.141A=	NP_001269314.1:p.Arg47=
NM_001320.6:c.141A=	NP_001311.3:p.Arg47=
NM_001320.7:c.141A= MANE Select	NP_001311.3:p.Arg47=
NM_001282385.2:c.141A=	NP_001269314.1:p.Arg47=