Canonical Allele Identifier: CA209839

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 210275
• ClinVar RCV Id: RCV000195185 ; RCV000520794
• dbSNP Id: rs753933273
• COSMIC: COSM1634598 ; COSM1634599
• MyVariant Identifiers: chr6:g.157405907C>T (hg19) ; chr6:g.157084773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084773C>T , CM000668.2:g.157084773C>T	GRCh38
NC_000006.11:g.157405907C>T , CM000668.1:g.157405907C>T	GRCh37
NC_000006.10:g.157447599C>T	NCBI36
NG_032093.1:g.311844C>T
NG_032093.2:g.311844C>T
NG_066624.1:g.313748C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.2359C>T	ENSP00000055163.8:p.Gln787Ter
ENST00000414678.8:c.2359C>T	ENSP00000412835.3:p.Gln787Ter
ENST00000637015.2:c.2359C>T	ENSP00000489729.2:p.Gln787Ter
ENST00000319584.11:c.373C>T	ENSP00000313006.7:p.Gln125Ter
ENST00000346085.10:c.2398C>T	ENSP00000344546.5:p.Gln800Ter
ENST00000350026.10:c.2110C>T	ENSP00000055163.7:p.Gln704Ter
ENST00000414678.7:c.607C>T	ENSP00000412835.2:p.Gln203Ter
ENST00000452544.2:n.260C>T
ENST00000493658.2:n.8C>T
ENST00000635849.1:c.-141C>T	ENSP00000490948.1:n.-141C>T
ENST00000636930.2:c.2359C>T MANE Select	ENSP00000490491.2:p.Gln787Ter
ENST00000637003.1:c.-141C>T	ENSP00000489666.1:n.-141C>T
ENST00000637810.1:c.-141C>T	ENSP00000489636.1:n.-141C>T
ENST00000637904.1:c.-141C>T	ENSP00000490550.1:n.-141C>T
ENST00000647938.1:c.2149C>T	ENSP00000498155.1:p.Gln717Ter
ENST00000674190.1:n.1108C>T
ENST00000319584.10:c.376C>T	ENSP00000313006.6:p.Gln126Ter
ENST00000346085.9:c.2149C>T	ENSP00000344546.4:p.Gln717Ter
ENST00000350026.9:c.2110C>T	ENSP00000055163.7:p.Gln704Ter
ENST00000414678.6:c.607C>T	ENSP00000412835.2:p.Gln203Ter
ENST00000452544.1:n.218C>T
ENST00000493658.1:n.8C>T
NM_017519.2:c.2110C>T	NP_059989.2:p.Gln704Ter
NM_020732.3:c.2149C>T	NP_065783.3:p.Gln717Ter
XM_005267069.3:c.2110C>T	XP_005267126.2:p.Gln704Ter
XM_011535984.1:c.1060C>T	XP_011534286.1:p.Gln354Ter
XM_011535985.1:c.1060C>T	XP_011534287.1:p.Gln354Ter
XM_011535986.1:c.640C>T	XP_011534288.1:p.Gln214Ter
XM_011535987.1:c.259C>T	XP_011534289.1:p.Gln87Ter
NM_001346813.1:c.2110C>T	NP_001333742.1:p.Gln704Ter
NM_001363725.1:c.-141C>T	NP_001350654.1:n.-141C>T
XM_011535984.2:c.2191C>T	XP_011534286.2:p.Gln731Ter
XM_017011103.2:c.2191C>T	XP_016866592.1:p.Gln731Ter
XM_017011104.1:c.2191C>T	XP_016866593.1:p.Gln731Ter
XM_017011105.2:c.2191C>T	XP_016866594.1:p.Gln731Ter
XM_017011106.2:c.2191C>T	XP_016866595.1:p.Gln731Ter
XM_017011107.2:c.2191C>T	XP_016866596.1:p.Gln731Ter
XR_002956289.1:n.2274C>T
NM_001363725.2:c.-141C>T	NP_001350654.1:n.-141C>T
NM_001371656.1:c.2398C>T	NP_001358585.1:p.Gln800Ter
NM_001374820.1:c.2398C>T	NP_001361749.1:p.Gln800Ter
NM_001374828.1:c.2359C>T MANE Select	NP_001361757.1:p.Gln787Ter
NM_017519.3:c.2359C>T	NP_059989.3:p.Gln787Ter