Canonical Allele Identifier: CA363471999

Gene: CSNK2B

Linked Data

• ClinVar Variation Id: 2229410
• ClinVar RCV Id: RCV002712549
• gnomAD v4: 6-31667911-T-C
• MyVariant Identifiers: chr6:g.31635688T>C (hg19) ; chr6:g.31667911T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31667911T>C , CM000668.2:g.31667911T>C	GRCh38
NC_000006.11:g.31635688T>C , CM000668.1:g.31635688T>C	GRCh37
NC_000006.10:g.31743667T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375882.7:c.116T>C MANE Select	ENSP00000365042.3:p.Leu39Pro
ENST00000465481.6:n.249T>C
ENST00000475875.2:n.1199T>C
ENST00000677388.1:c.173T>C	ENSP00000504290.1:p.Leu58Pro
ENST00000677536.1:c.173T>C	ENSP00000502967.1:p.Leu58Pro
ENST00000677758.1:c.173T>C	ENSP00000504242.1:p.Leu58Pro
ENST00000375865.6:c.116T>C	ENSP00000365025.2:p.Leu39Pro
ENST00000375866.2:c.116T>C	ENSP00000365026.2:p.Leu39Pro
ENST00000375880.6:c.116T>C	ENSP00000365040.2:p.Leu39Pro
ENST00000375882.6:c.116T>C	ENSP00000365042.2:p.Leu39Pro
ENST00000375885.8:c.173T>C	ENSP00000365046.4:p.Leu58Pro
ENST00000465481.5:n.249T>C
ENST00000468255.5:n.255T>C
ENST00000481269.1:n.242T>C
ENST00000617558.2:c.116T>C	ENSP00000483989.2:p.Leu39Pro
NM_001282385.1:c.116T>C	NP_001269314.1:p.Leu39Pro
NM_001320.6:c.116T>C	NP_001311.3:p.Leu39Pro
NM_001320.7:c.116T>C MANE Select	NP_001311.3:p.Leu39Pro
NM_001282385.2:c.116T>C	NP_001269314.1:p.Leu39Pro