Canonical Allele Identifier: CA1675523562

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201402G= , CM000668.2:g.157201402G=	GRCh38
NC_000006.11:g.157522536G= , CM000668.1:g.157522536G=	GRCh37
NC_000006.10:g.157564228G=	NCBI36
NG_032093.1:g.428473G=
NG_032093.2:g.428473G=
NG_066624.1:g.430377G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5018G=	ENSP00000055163.8:p.Arg1673=
ENST00000414678.8:c.5087G=	ENSP00000412835.3:p.Arg1696=
ENST00000637015.2:c.5306G=	ENSP00000489729.2:p.Arg1769=
ENST00000346085.10:c.5057G=	ENSP00000344546.5:p.Arg1686=
ENST00000350026.10:c.4769G=	ENSP00000055163.7:p.Arg1590=
ENST00000414678.7:c.3335G=	ENSP00000412835.2:p.Arg1112=
ENST00000635849.1:c.2498G=	ENSP00000490948.1:p.Arg833=
ENST00000635957.1:c.2129G=	ENSP00000490385.1:p.Arg710=
ENST00000636227.1:n.3640G=
ENST00000636254.1:n.1097G=
ENST00000636930.2:c.5177G= MANE Select	ENSP00000490491.2:p.Arg1726=
ENST00000636940.1:n.3174G=
ENST00000637015.1:c.2545G=
ENST00000637568.1:c.2459G=
ENST00000637741.1:n.1843G=
ENST00000637810.1:c.2519G=	ENSP00000489636.1:p.Arg840=
ENST00000637904.1:c.2678G=	ENSP00000490550.1:p.Arg893=
ENST00000647938.1:c.4808G=	ENSP00000498155.1:p.Arg1603=
ENST00000346085.9:c.4808G=	ENSP00000344546.4:p.Arg1603=
ENST00000350026.9:c.4769G=	ENSP00000055163.7:p.Arg1590=
ENST00000414678.6:c.3335G=	ENSP00000412835.2:p.Arg1112=
NM_017519.2:c.4769G=	NP_059989.2:p.Arg1590=
NM_020732.3:c.4808G=	NP_065783.3:p.Arg1603=
XM_005267069.3:c.4928G=	XP_005267126.2:p.Arg1643=
XM_011535984.1:c.4007G=	XP_011534286.1:p.Arg1336=
XM_011535985.1:c.3827G=	XP_011534287.1:p.Arg1276=
XM_011535986.1:c.3587G=	XP_011534288.1:p.Arg1196=
XM_011535987.1:c.3206G=	XP_011534289.1:p.Arg1069=
XM_011535988.1:c.2069G=	XP_011534290.1:p.Arg690=
NM_001346813.1:c.4928G=	NP_001333742.1:p.Arg1643=
NM_001363725.1:c.2678G=	NP_001350654.1:p.Arg893=
XM_011535984.2:c.5138G=	XP_011534286.2:p.Arg1713=
XM_011535988.3:c.2069G=	XP_011534290.1:p.Arg690=
XM_017011103.2:c.5039G=	XP_016866592.1:p.Arg1680=
XM_017011104.1:c.5009G=	XP_016866593.1:p.Arg1670=
XM_017011105.2:c.4979G=	XP_016866594.1:p.Arg1660=
XM_017011106.2:c.4850G=	XP_016866595.1:p.Arg1617=
XM_017011107.2:c.4829G=	XP_016866596.1:p.Arg1610=
XR_002956289.1:n.5124G=
NM_001363725.2:c.2678G=	NP_001350654.1:p.Arg893=
NM_001371656.1:c.5057G=	NP_001358585.1:p.Arg1686=
NM_001374820.1:c.5057G=	NP_001361749.1:p.Arg1686=
NM_001374828.1:c.5177G= MANE Select	NP_001361757.1:p.Arg1726=
NM_017519.3:c.5018G=	NP_059989.3:p.Arg1673=