Canonical Allele Identifier: CA1675522818

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201028G= , CM000668.2:g.157201028G=	GRCh38
NC_000006.11:g.157522162G= , CM000668.1:g.157522162G=	GRCh37
NC_000006.10:g.157563854G=	NCBI36
NG_032093.1:g.428099G=
NG_032093.2:g.428099G=
NG_066624.1:g.430003G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4644G=	ENSP00000055163.8:p.Arg1548=
ENST00000414678.8:c.4713G=	ENSP00000412835.3:p.Arg1571=
ENST00000637015.2:c.4932G=	ENSP00000489729.2:p.Arg1644=
ENST00000346085.10:c.4683G=	ENSP00000344546.5:p.Arg1561=
ENST00000350026.10:c.4395G=	ENSP00000055163.7:p.Arg1465=
ENST00000414678.7:c.2961G=	ENSP00000412835.2:p.Arg987=
ENST00000635849.1:c.2124G=	ENSP00000490948.1:p.Arg708=
ENST00000635957.1:c.1755G=	ENSP00000490385.1:p.Arg585=
ENST00000636227.1:n.3266G=
ENST00000636254.1:n.723G=
ENST00000636930.2:c.4803G= MANE Select	ENSP00000490491.2:p.Arg1601=
ENST00000636940.1:n.2800G=
ENST00000637015.1:c.2171G=
ENST00000637568.1:c.2085G=
ENST00000637741.1:n.1469G=
ENST00000637810.1:c.2145G=	ENSP00000489636.1:p.Arg715=
ENST00000637904.1:c.2304G=	ENSP00000490550.1:p.Arg768=
ENST00000647938.1:c.4434G=	ENSP00000498155.1:p.Arg1478=
ENST00000346085.9:c.4434G=	ENSP00000344546.4:p.Arg1478=
ENST00000350026.9:c.4395G=	ENSP00000055163.7:p.Arg1465=
ENST00000414678.6:c.2961G=	ENSP00000412835.2:p.Arg987=
NM_017519.2:c.4395G=	NP_059989.2:p.Arg1465=
NM_020732.3:c.4434G=	NP_065783.3:p.Arg1478=
XM_005267069.3:c.4554G=	XP_005267126.2:p.Arg1518=
XM_011535984.1:c.3633G=	XP_011534286.1:p.Arg1211=
XM_011535985.1:c.3453G=	XP_011534287.1:p.Arg1151=
XM_011535986.1:c.3213G=	XP_011534288.1:p.Arg1071=
XM_011535987.1:c.2832G=	XP_011534289.1:p.Arg944=
XM_011535988.1:c.1695G=	XP_011534290.1:p.Arg565=
NM_001346813.1:c.4554G=	NP_001333742.1:p.Arg1518=
NM_001363725.1:c.2304G=	NP_001350654.1:p.Arg768=
XM_011535984.2:c.4764G=	XP_011534286.2:p.Arg1588=
XM_011535988.3:c.1695G=	XP_011534290.1:p.Arg565=
XM_017011103.2:c.4665G=	XP_016866592.1:p.Arg1555=
XM_017011104.1:c.4635G=	XP_016866593.1:p.Arg1545=
XM_017011105.2:c.4605G=	XP_016866594.1:p.Arg1535=
XM_017011106.2:c.4476G=	XP_016866595.1:p.Arg1492=
XM_017011107.2:c.4455G=	XP_016866596.1:p.Arg1485=
XR_002956289.1:n.4750G=
NM_001363725.2:c.2304G=	NP_001350654.1:p.Arg768=
NM_001371656.1:c.4683G=	NP_001358585.1:p.Arg1561=
NM_001374820.1:c.4683G=	NP_001361749.1:p.Arg1561=
NM_001374828.1:c.4803G= MANE Select	NP_001361757.1:p.Arg1601=
NM_017519.3:c.4644G=	NP_059989.3:p.Arg1548=