Canonical Allele Identifier: CA3718589

Gene: CSNK2B

Linked Data

• dbSNP Id: rs760173426
• ExAC: 6:31635789 AT / A
• gnomAD v2: 6-31635789-AT-A
• gnomAD v4: 6-31668012-AT-A
• MyVariant Identifiers: chr6:g.31635790del (hg19) ; chr6:g.31668014del (hg38) ; chr6:g.31668013del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31668017del , CM000668.2:g.31668017del	GRCh38
NC_000006.11:g.31635794del , CM000668.1:g.31635794del	GRCh37
NC_000006.10:g.31743773del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375882.7:c.175+47del MANE Select	ENSP00000365042.3:n.175+47del
ENST00000465481.6:n.355del
ENST00000475875.2:n.1305del
ENST00000677388.1:c.232+47del	ENSP00000504290.1:n.232+47del
ENST00000677536.1:c.232+47del	ENSP00000502967.1:n.232+47del
ENST00000677758.1:c.232+47del	ENSP00000504242.1:n.232+47del
ENST00000375865.6:c.175+47del	ENSP00000365025.2:n.175+47del
ENST00000375866.2:c.175+47del	ENSP00000365026.2:n.175+47del
ENST00000375880.6:c.175+47del	ENSP00000365040.2:n.175+47del
ENST00000375882.6:c.175+47del	ENSP00000365042.2:n.175+47del
ENST00000375885.8:c.232+47del	ENSP00000365046.4:n.232+47del
ENST00000465481.5:n.355del
ENST00000468255.5:n.314+47del
ENST00000481269.1:n.301+47del
ENST00000617558.2:c.175+47del	ENSP00000483989.2:n.175+47del
NM_001282385.1:c.175+47del	NP_001269314.1:n.175+47del
NM_001320.6:c.175+47del	NP_001311.3:n.175+47del
NM_001320.7:c.175+47del MANE Select	NP_001311.3:n.175+47del
NM_001282385.2:c.175+47del	NP_001269314.1:n.175+47del