Canonical Allele Identifier: CA363472204

Gene: CSNK2B

Linked Data

• ClinVar Variation Id: 426599
• ClinVar RCV Id: RCV001267434 ; RCV001281589 ; RCV002468581 ; RCV003942606
• dbSNP Id: rs1085307703
• MyVariant Identifiers: chr6:g.31635711C>T (hg19) ; chr6:g.31667934C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31667934C>T , CM000668.2:g.31667934C>T	GRCh38
NC_000006.11:g.31635711C>T , CM000668.1:g.31635711C>T	GRCh37
NC_000006.10:g.31743690C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375882.7:c.139C>T MANE Select	ENSP00000365042.3:p.Arg47Ter
ENST00000465481.6:n.272C>T
ENST00000475875.2:n.1222C>T
ENST00000677388.1:c.196C>T	ENSP00000504290.1:p.Arg66Ter
ENST00000677536.1:c.196C>T	ENSP00000502967.1:p.Arg66Ter
ENST00000677758.1:c.196C>T	ENSP00000504242.1:p.Arg66Ter
ENST00000375865.6:c.139C>T	ENSP00000365025.2:p.Arg47Ter
ENST00000375866.2:c.139C>T	ENSP00000365026.2:p.Arg47Ter
ENST00000375880.6:c.139C>T	ENSP00000365040.2:p.Arg47Ter
ENST00000375882.6:c.139C>T	ENSP00000365042.2:p.Arg47Ter
ENST00000375885.8:c.196C>T	ENSP00000365046.4:p.Arg66Ter
ENST00000465481.5:n.272C>T
ENST00000468255.5:n.278C>T
ENST00000481269.1:n.265C>T
ENST00000617558.2:c.139C>T	ENSP00000483989.2:p.Arg47Ter
NM_001282385.1:c.139C>T	NP_001269314.1:p.Arg47Ter
NM_001320.6:c.139C>T	NP_001311.3:p.Arg47Ter
NM_001320.7:c.139C>T MANE Select	NP_001311.3:p.Arg47Ter
NM_001282385.2:c.139C>T	NP_001269314.1:p.Arg47Ter