Canonical Allele Identifier: CA281638352

Gene: CSNK2A2

Linked Data

• dbSNP Id: rs920473948
• gnomAD v3: 16-58175284-C-T
• gnomAD v4: 16-58175284-C-T
• MyVariant Identifiers: chr16:g.58209188C>T (hg19) ; chr16:g.58175284C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58175284C>T , CM000678.2:g.58175284C>T	GRCh38
NC_000016.9:g.58209188C>T , CM000678.1:g.58209188C>T	GRCh37
NC_000016.8:g.56766689C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262506.8:c.370-774G>A MANE Select	ENSP00000262506.3:n.370-774G>A
ENST00000563307.2:n.2179-774G>A
ENST00000565188.2:c.217-774G>A	ENSP00000454874.2:n.217-774G>A
ENST00000677823.1:n.2179-774G>A
ENST00000262506.7:c.370-774G>A	ENSP00000262506.3:n.370-774G>A
ENST00000562367.1:n.195-774G>A
ENST00000565188.1:c.370-774G>A	ENSP00000454874.1:n.370-774G>A
ENST00000566813.5:n.422-774G>A
ENST00000567730.6:c.154-7489G>A	ENSP00000456606.2:n.154-7489G>A
NM_001896.2:c.370-774G>A	NP_001887.1:n.370-774G>A
XM_005255800.2:c.217-774G>A	XP_005255857.1:n.217-774G>A
XM_005255801.2:c.-42-774G>A	XP_005255858.1:n.-42-774G>A
NM_001896.3:c.370-774G>A	NP_001887.1:n.370-774G>A
XM_005255800.4:c.217-774G>A	XP_005255857.1:n.217-774G>A
XM_005255801.3:c.-42-774G>A	XP_005255858.1:n.-42-774G>A
NM_001896.4:c.370-774G>A MANE Select	NP_001887.1:n.370-774G>A