Canonical Allele Identifier: CA363471873

Gene: CSNK2B

Linked Data

• ClinVar Variation Id: 1275774
• ClinVar RCV Id: RCV001682651
• dbSNP Id: rs1374628000
• gnomAD v2: 6-31635673-T-G
• gnomAD v4: 6-31667896-T-G
• COSMIC: COSM5710060
• MyVariant Identifiers: chr6:g.31635673T>G (hg19) ; chr6:g.31667896T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31667896T>G , CM000668.2:g.31667896T>G	GRCh38
NC_000006.11:g.31635673T>G , CM000668.1:g.31635673T>G	GRCh37
NC_000006.10:g.31743652T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375882.7:c.101T>G MANE Select	ENSP00000365042.3:p.Phe34Cys
ENST00000465481.6:n.234T>G
ENST00000475875.2:n.1184T>G
ENST00000677388.1:c.158T>G	ENSP00000504290.1:p.Phe53Cys
ENST00000677536.1:c.158T>G	ENSP00000502967.1:p.Phe53Cys
ENST00000677758.1:c.158T>G	ENSP00000504242.1:p.Phe53Cys
ENST00000375865.6:c.101T>G	ENSP00000365025.2:p.Phe34Cys
ENST00000375866.2:c.101T>G	ENSP00000365026.2:p.Phe34Cys
ENST00000375880.6:c.101T>G	ENSP00000365040.2:p.Phe34Cys
ENST00000375882.6:c.101T>G	ENSP00000365042.2:p.Phe34Cys
ENST00000375885.8:c.158T>G	ENSP00000365046.4:p.Phe53Cys
ENST00000465481.5:n.234T>G
ENST00000468255.5:n.240T>G
ENST00000481269.1:n.227T>G
ENST00000617558.2:c.101T>G	ENSP00000483989.2:p.Phe34Cys
NM_001282385.1:c.101T>G	NP_001269314.1:p.Phe34Cys
NM_001320.6:c.101T>G	NP_001311.3:p.Phe34Cys
NM_001320.7:c.101T>G MANE Select	NP_001311.3:p.Phe34Cys
NM_001282385.2:c.101T>G	NP_001269314.1:p.Phe34Cys