Canonical Allele Identifier: CA363473745

Gene: CSNK2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31668652A>G , CM000668.2:g.31668652A>G	GRCh38
NC_000006.11:g.31636429A>G , CM000668.1:g.31636429A>G	GRCh37
NC_000006.10:g.31744408A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001320.7:c.289A>G MANE Select	NP_001311.3:p.Met97Val
ENST00000375882.7:c.289A>G MANE Select	ENSP00000365042.3:p.Met97Val
NM_001282385.1:c.289A>G	NP_001269314.1:p.Met97Val
NM_001282385.2:c.289A>G	NP_001269314.1:p.Met97Val
NM_001320.6:c.289A>G	NP_001311.3:p.Met97Val
ENST00000375865.6:c.289A>G	ENSP00000365025.2:p.Met97Val
ENST00000375866.2:c.289A>G	ENSP00000365026.2:p.Met97Val
ENST00000375880.6:c.289A>G	ENSP00000365040.2:p.Met97Val
ENST00000375882.6:c.289A>G	ENSP00000365042.2:p.Met97Val
ENST00000375885.8:c.346A>G	ENSP00000365046.4:p.Met116Val
ENST00000465481.6:n.990A>G
ENST00000468255.5:n.428A>G
ENST00000475875.2:n.1940A>G
ENST00000481269.1:n.415A>G
ENST00000617558.2:c.289A>G	ENSP00000483989.2:p.Met97Val
ENST00000677388.1:c.*75A>G	ENSP00000504290.1:n.*75A>G
ENST00000677536.1:c.346A>G	ENSP00000502967.1:p.Met116Val
ENST00000677758.1:c.346A>G	ENSP00000504242.1:p.Met116Val