Canonical Allele Identifier: CA452781591

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339621
• COSMIC: COSM4663249 ; COSM4663250
• MyVariant Identifiers: chr6:g.157511190G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190056G>A , CM000668.2:g.157190056G>A	GRCh38
NC_000006.11:g.157511190G>A , CM000668.1:g.157511190G>A	GRCh37
NC_000006.10:g.157552882G>A	NCBI36
NG_032093.1:g.417127G>A
NG_032093.2:g.417127G>A
NG_066624.1:g.419031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3918G>A	ENSP00000055163.8:p.Val1306=
ENST00000414678.8:c.3987G>A	ENSP00000412835.3:p.Val1329=
ENST00000637015.2:c.4206G>A	ENSP00000489729.2:p.Val1402=
ENST00000346085.10:c.3957G>A	ENSP00000344546.5:p.Val1319=
ENST00000350026.10:c.3669G>A	ENSP00000055163.7:p.Val1223=
ENST00000414678.7:c.2235G>A	ENSP00000412835.2:p.Val745=
ENST00000635849.1:c.1398G>A	ENSP00000490948.1:p.Val466=
ENST00000635957.1:c.1029G>A	ENSP00000490385.1:p.Val343=
ENST00000636930.2:c.4077G>A MANE Select	ENSP00000490491.2:p.Val1359=
ENST00000636940.1:n.2074G>A
ENST00000637015.1:c.1445G>A
ENST00000637568.1:c.1359G>A
ENST00000637741.1:n.743G>A
ENST00000637810.1:c.1419G>A	ENSP00000489636.1:p.Val473=
ENST00000637904.1:c.1578G>A	ENSP00000490550.1:p.Val526=
ENST00000647938.1:c.3708G>A	ENSP00000498155.1:p.Val1236=
ENST00000346085.9:c.3708G>A	ENSP00000344546.4:p.Val1236=
ENST00000350026.9:c.3669G>A	ENSP00000055163.7:p.Val1223=
ENST00000414678.6:c.2235G>A	ENSP00000412835.2:p.Val745=
NM_017519.2:c.3669G>A	NP_059989.2:p.Val1223=
NM_020732.3:c.3708G>A	NP_065783.3:p.Val1236=
XM_005267069.3:c.3828G>A	XP_005267126.2:p.Val1276=
XM_011535984.1:c.2907G>A	XP_011534286.1:p.Val969=
XM_011535985.1:c.2727G>A	XP_011534287.1:p.Val909=
XM_011535986.1:c.2487G>A	XP_011534288.1:p.Val829=
XM_011535987.1:c.2106G>A	XP_011534289.1:p.Val702=
XM_011535988.1:c.969G>A	XP_011534290.1:p.Val323=
NM_001346813.1:c.3828G>A	NP_001333742.1:p.Val1276=
NM_001363725.1:c.1578G>A	NP_001350654.1:p.Val526=
XM_011535984.2:c.4038G>A	XP_011534286.2:p.Val1346=
XM_011535988.3:c.969G>A	XP_011534290.1:p.Val323=
XM_017011103.2:c.3939G>A	XP_016866592.1:p.Val1313=
XM_017011104.1:c.3909G>A	XP_016866593.1:p.Val1303=
XM_017011105.2:c.3879G>A	XP_016866594.1:p.Val1293=
XM_017011106.2:c.3750G>A	XP_016866595.1:p.Val1250=
XM_017011107.2:c.3729G>A	XP_016866596.1:p.Val1243=
XR_002956289.1:n.4121G>A
NM_001363725.2:c.1578G>A	NP_001350654.1:p.Val526=
NM_001371656.1:c.3957G>A	NP_001358585.1:p.Val1319=
NM_001374820.1:c.3957G>A	NP_001361749.1:p.Val1319=
NM_001374828.1:c.4077G>A MANE Select	NP_001361757.1:p.Val1359=
NM_017519.3:c.3918G>A	NP_059989.3:p.Val1306=