Canonical Allele Identifier: CA363469433

Gene: CSNK2B

Linked Data

• ClinVar Variation Id: 489241
• ClinVar RCV Id: RCV000578649 ; RCV003448326
• dbSNP Id: rs1554169462
• MyVariant Identifiers: chr6:g.31634644G>A (hg19) ; chr6:g.31666867G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31666867G>A , CM000668.2:g.31666867G>A	GRCh38
NC_000006.11:g.31634644G>A , CM000668.1:g.31634644G>A	GRCh37
NC_000006.10:g.31742623G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375882.7:c.36G>A MANE Select	ENSP00000365042.3:p.Trp12Ter
ENST00000465481.6:n.169G>A
ENST00000475875.2:n.155G>A
ENST00000677388.1:c.93G>A	ENSP00000504290.1:p.Trp31Ter
ENST00000677536.1:c.93G>A	ENSP00000502967.1:p.Trp31Ter
ENST00000677758.1:c.93G>A	ENSP00000504242.1:p.Trp31Ter
ENST00000375865.6:c.36G>A	ENSP00000365025.2:p.Trp12Ter
ENST00000375866.2:c.36G>A	ENSP00000365026.2:p.Trp12Ter
ENST00000375880.6:c.36G>A	ENSP00000365040.2:p.Trp12Ter
ENST00000375882.6:c.36G>A	ENSP00000365042.2:p.Trp12Ter
ENST00000375885.8:c.93G>A	ENSP00000365046.4:p.Trp31Ter
ENST00000465481.5:n.169G>A
ENST00000468255.5:n.175G>A
ENST00000475875.1:n.155G>A
ENST00000481269.1:n.162G>A
ENST00000617558.2:c.36G>A	ENSP00000483989.2:p.Trp12Ter
NM_001282385.1:c.36G>A	NP_001269314.1:p.Trp12Ter
NM_001320.6:c.36G>A	NP_001311.3:p.Trp12Ter
NM_001320.7:c.36G>A MANE Select	NP_001311.3:p.Trp12Ter
NM_001282385.2:c.36G>A	NP_001269314.1:p.Trp12Ter