Canonical Allele Identifier: CA1139659898

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 988498
• ClinVar RCV Id: RCV001269883
• dbSNP Id: rs1794071513

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201060dup , CM000668.2:g.157201060dup	GRCh38
NC_000006.11:g.157522194dup , CM000668.1:g.157522194dup	GRCh37
NC_000006.10:g.157563886dup	NCBI36
NG_032093.1:g.428131dup
NG_032093.2:g.428131dup
NG_066624.1:g.430035dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4676dup	ENSP00000055163.8:p.Tyr1560LeufsTer20
ENST00000414678.8:c.4745dup	ENSP00000412835.3:p.Tyr1583LeufsTer20
ENST00000637015.2:c.4964dup	ENSP00000489729.2:p.Tyr1656LeufsTer20
ENST00000346085.10:c.4715dup	ENSP00000344546.5:p.Tyr1573LeufsTer20
ENST00000350026.10:c.4427dup	ENSP00000055163.7:p.Tyr1477LeufsTer20
ENST00000414678.7:c.2993dup	ENSP00000412835.2:p.Tyr999LeufsTer20
ENST00000635849.1:c.2156dup	ENSP00000490948.1:p.Tyr720LeufsTer20
ENST00000635957.1:c.1787dup	ENSP00000490385.1:p.Tyr597LeufsTer20
ENST00000636227.1:n.3298dup
ENST00000636254.1:n.755dup
ENST00000636930.2:c.4835dup MANE Select	ENSP00000490491.2:p.Tyr1613LeufsTer20
ENST00000636940.1:n.2832dup
ENST00000637015.1:c.2203dup
ENST00000637568.1:c.2117dup
ENST00000637741.1:n.1501dup
ENST00000637810.1:c.2177dup	ENSP00000489636.1:p.Tyr727LeufsTer20
ENST00000637904.1:c.2336dup	ENSP00000490550.1:p.Tyr780LeufsTer20
ENST00000647938.1:c.4466dup	ENSP00000498155.1:p.Tyr1490LeufsTer20
ENST00000346085.9:c.4466dup	ENSP00000344546.4:p.Tyr1490LeufsTer20
ENST00000350026.9:c.4427dup	ENSP00000055163.7:p.Tyr1477LeufsTer20
ENST00000414678.6:c.2993dup	ENSP00000412835.2:p.Tyr999LeufsTer20
NM_017519.2:c.4427dup	NP_059989.2:p.Tyr1477LeufsTer20
NM_020732.3:c.4466dup	NP_065783.3:p.Tyr1490LeufsTer20
XM_005267069.3:c.4586dup	XP_005267126.2:p.Tyr1530LeufsTer20
XM_011535984.1:c.3665dup	XP_011534286.1:p.Tyr1223LeufsTer20
XM_011535985.1:c.3485dup	XP_011534287.1:p.Tyr1163LeufsTer20
XM_011535986.1:c.3245dup	XP_011534288.1:p.Tyr1083LeufsTer20
XM_011535987.1:c.2864dup	XP_011534289.1:p.Tyr956LeufsTer20
XM_011535988.1:c.1727dup	XP_011534290.1:p.Tyr577LeufsTer20
NM_001346813.1:c.4586dup	NP_001333742.1:p.Tyr1530LeufsTer20
NM_001363725.1:c.2336dup	NP_001350654.1:p.Tyr780LeufsTer20
XM_011535984.2:c.4796dup	XP_011534286.2:p.Tyr1600LeufsTer20
XM_011535988.3:c.1727dup	XP_011534290.1:p.Tyr577LeufsTer20
XM_017011103.2:c.4697dup	XP_016866592.1:p.Tyr1567LeufsTer20
XM_017011104.1:c.4667dup	XP_016866593.1:p.Tyr1557LeufsTer20
XM_017011105.2:c.4637dup	XP_016866594.1:p.Tyr1547LeufsTer20
XM_017011106.2:c.4508dup	XP_016866595.1:p.Tyr1504LeufsTer20
XM_017011107.2:c.4487dup	XP_016866596.1:p.Tyr1497LeufsTer20
XR_002956289.1:n.4782dup
NM_001363725.2:c.2336dup	NP_001350654.1:p.Tyr780LeufsTer20
NM_001371656.1:c.4715dup	NP_001358585.1:p.Tyr1573LeufsTer20
NM_001374820.1:c.4715dup	NP_001361749.1:p.Tyr1573LeufsTer20
NM_001374828.1:c.4835dup MANE Select	NP_001361757.1:p.Tyr1613LeufsTer20
NM_017519.3:c.4676dup	NP_059989.3:p.Tyr1560LeufsTer20