Canonical Allele Identifier: CA1675523009

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201119G= , CM000668.2:g.157201119G=	GRCh38
NC_000006.11:g.157522253G= , CM000668.1:g.157522253G=	GRCh37
NC_000006.10:g.157563945G=	NCBI36
NG_032093.1:g.428190G=
NG_032093.2:g.428190G=
NG_066624.1:g.430094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4735G=	ENSP00000055163.8:p.Glu1579=
ENST00000414678.8:c.4804G=	ENSP00000412835.3:p.Glu1602=
ENST00000637015.2:c.5023G=	ENSP00000489729.2:p.Glu1675=
ENST00000346085.10:c.4774G=	ENSP00000344546.5:p.Glu1592=
ENST00000350026.10:c.4486G=	ENSP00000055163.7:p.Glu1496=
ENST00000414678.7:c.3052G=	ENSP00000412835.2:p.Glu1018=
ENST00000635849.1:c.2215G=	ENSP00000490948.1:p.Glu739=
ENST00000635957.1:c.1846G=	ENSP00000490385.1:p.Glu616=
ENST00000636227.1:n.3357G=
ENST00000636254.1:n.814G=
ENST00000636930.2:c.4894G= MANE Select	ENSP00000490491.2:p.Glu1632=
ENST00000636940.1:n.2891G=
ENST00000637015.1:c.2262G=
ENST00000637568.1:c.2176G=
ENST00000637741.1:n.1560G=
ENST00000637810.1:c.2236G=	ENSP00000489636.1:p.Glu746=
ENST00000637904.1:c.2395G=	ENSP00000490550.1:p.Glu799=
ENST00000647938.1:c.4525G=	ENSP00000498155.1:p.Glu1509=
ENST00000346085.9:c.4525G=	ENSP00000344546.4:p.Glu1509=
ENST00000350026.9:c.4486G=	ENSP00000055163.7:p.Glu1496=
ENST00000414678.6:c.3052G=	ENSP00000412835.2:p.Glu1018=
NM_017519.2:c.4486G=	NP_059989.2:p.Glu1496=
NM_020732.3:c.4525G=	NP_065783.3:p.Glu1509=
XM_005267069.3:c.4645G=	XP_005267126.2:p.Glu1549=
XM_011535984.1:c.3724G=	XP_011534286.1:p.Glu1242=
XM_011535985.1:c.3544G=	XP_011534287.1:p.Glu1182=
XM_011535986.1:c.3304G=	XP_011534288.1:p.Glu1102=
XM_011535987.1:c.2923G=	XP_011534289.1:p.Glu975=
XM_011535988.1:c.1786G=	XP_011534290.1:p.Glu596=
NM_001346813.1:c.4645G=	NP_001333742.1:p.Glu1549=
NM_001363725.1:c.2395G=	NP_001350654.1:p.Glu799=
XM_011535984.2:c.4855G=	XP_011534286.2:p.Glu1619=
XM_011535988.3:c.1786G=	XP_011534290.1:p.Glu596=
XM_017011103.2:c.4756G=	XP_016866592.1:p.Glu1586=
XM_017011104.1:c.4726G=	XP_016866593.1:p.Glu1576=
XM_017011105.2:c.4696G=	XP_016866594.1:p.Glu1566=
XM_017011106.2:c.4567G=	XP_016866595.1:p.Glu1523=
XM_017011107.2:c.4546G=	XP_016866596.1:p.Glu1516=
XR_002956289.1:n.4841G=
NM_001363725.2:c.2395G=	NP_001350654.1:p.Glu799=
NM_001371656.1:c.4774G=	NP_001358585.1:p.Glu1592=
NM_001374820.1:c.4774G=	NP_001361749.1:p.Glu1592=
NM_001374828.1:c.4894G= MANE Select	NP_001361757.1:p.Glu1632=
NM_017519.3:c.4735G=	NP_059989.3:p.Glu1579=