Canonical Allele Identifier: CA1675543218

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207265G= , CM000668.2:g.157207265G=	GRCh38
NC_000006.11:g.157528399G= , CM000668.1:g.157528399G=	GRCh37
NC_000006.10:g.157570091G=	NCBI36
NG_032093.1:g.434336G=
NG_032093.2:g.434336G=
NG_066624.1:g.436240G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6493G= MANE Select	NP_001361757.1:p.Glu2165=
ENST00000636930.2:c.6493G= MANE Select	ENSP00000490491.2:p.Glu2165=
NM_001346813.1:c.6244G=	NP_001333742.1:p.Glu2082=
NM_001363725.1:c.3994G=	NP_001350654.1:p.Glu1332=
NM_001363725.2:c.3994G=	NP_001350654.1:p.Glu1332=
NM_001371656.1:c.6373G=	NP_001358585.1:p.Glu2125=
NM_001374820.1:c.6373G=	NP_001361749.1:p.Glu2125=
NM_017519.2:c.6085G=	NP_059989.2:p.Glu2029=
NM_017519.3:c.6334G=	NP_059989.3:p.Glu2112=
NM_020732.3:c.6124G=	NP_065783.3:p.Glu2042=
ENST00000346085.10:c.6373G=	ENSP00000344546.5:p.Glu2125=
ENST00000346085.9:c.6124G=	ENSP00000344546.4:p.Glu2042=
ENST00000350026.10:c.6085G=	ENSP00000055163.7:p.Glu2029=
ENST00000350026.11:c.6334G=	ENSP00000055163.8:p.Glu2112=
ENST00000350026.9:c.6085G=	ENSP00000055163.7:p.Glu2029=
ENST00000414678.6:c.4651G=	ENSP00000412835.2:p.Glu1551=
ENST00000414678.7:c.4651G=	ENSP00000412835.2:p.Glu1551=
ENST00000414678.8:c.6403G=	ENSP00000412835.3:p.Glu2135=
ENST00000635849.1:c.3814G=	ENSP00000490948.1:p.Glu1272=
ENST00000635928.1:c.649G=	ENSP00000489717.1:p.Glu217=
ENST00000635957.1:c.3445G=	ENSP00000490385.1:p.Glu1149=
ENST00000636227.1:n.4956G=
ENST00000636254.1:n.2413G=
ENST00000636940.1:n.4490G=
ENST00000637015.1:c.3861G=
ENST00000637015.2:c.6622G=	ENSP00000489729.2:p.Glu2208=
ENST00000637568.1:c.3775G=
ENST00000637741.1:n.3159G=
ENST00000637810.1:c.3835G=	ENSP00000489636.1:p.Glu1279=
ENST00000637904.1:c.3994G=	ENSP00000490550.1:p.Glu1332=
ENST00000637933.1:n.3608G=
ENST00000647938.1:c.6124G=	ENSP00000498155.1:p.Glu2042=
XM_005267069.3:c.6244G=	XP_005267126.2:p.Glu2082=
XM_011535984.1:c.5323G=	XP_011534286.1:p.Glu1775=
XM_011535984.2:c.6454G=	XP_011534286.2:p.Glu2152=
XM_011535985.1:c.5143G=	XP_011534287.1:p.Glu1715=
XM_011535986.1:c.4903G=	XP_011534288.1:p.Glu1635=
XM_011535987.1:c.4522G=	XP_011534289.1:p.Glu1508=
XM_011535988.1:c.3385G=	XP_011534290.1:p.Glu1129=
XM_011535988.3:c.3385G=	XP_011534290.1:p.Glu1129=
XM_017011103.2:c.6355G=	XP_016866592.1:p.Glu2119=
XM_017011104.1:c.6325G=	XP_016866593.1:p.Glu2109=
XM_017011105.2:c.6295G=	XP_016866594.1:p.Glu2099=
XM_017011106.2:c.6166G=	XP_016866595.1:p.Glu2056=
XM_017011107.2:c.6145G=	XP_016866596.1:p.Glu2049=
XR_002956289.1:n.6440G=