Canonical Allele Identifier: CA1675522806

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201002G= , CM000668.2:g.157201002G=	GRCh38
NC_000006.11:g.157522136G= , CM000668.1:g.157522136G=	GRCh37
NC_000006.10:g.157563828G=	NCBI36
NG_032093.1:g.428073G=
NG_032093.2:g.428073G=
NG_066624.1:g.429977G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4618G=	ENSP00000055163.8:p.Asp1540=
ENST00000414678.8:c.4687G=	ENSP00000412835.3:p.Asp1563=
ENST00000637015.2:c.4906G=	ENSP00000489729.2:p.Asp1636=
ENST00000346085.10:c.4657G=	ENSP00000344546.5:p.Asp1553=
ENST00000350026.10:c.4369G=	ENSP00000055163.7:p.Asp1457=
ENST00000414678.7:c.2935G=	ENSP00000412835.2:p.Asp979=
ENST00000635849.1:c.2098G=	ENSP00000490948.1:p.Asp700=
ENST00000635957.1:c.1729G=	ENSP00000490385.1:p.Asp577=
ENST00000636227.1:n.3240G=
ENST00000636254.1:n.697G=
ENST00000636930.2:c.4777G= MANE Select	ENSP00000490491.2:p.Asp1593=
ENST00000636940.1:n.2774G=
ENST00000637015.1:c.2145G=
ENST00000637568.1:c.2059G=
ENST00000637741.1:n.1443G=
ENST00000637810.1:c.2119G=	ENSP00000489636.1:p.Asp707=
ENST00000637904.1:c.2278G=	ENSP00000490550.1:p.Asp760=
ENST00000647938.1:c.4408G=	ENSP00000498155.1:p.Asp1470=
ENST00000346085.9:c.4408G=	ENSP00000344546.4:p.Asp1470=
ENST00000350026.9:c.4369G=	ENSP00000055163.7:p.Asp1457=
ENST00000414678.6:c.2935G=	ENSP00000412835.2:p.Asp979=
NM_017519.2:c.4369G=	NP_059989.2:p.Asp1457=
NM_020732.3:c.4408G=	NP_065783.3:p.Asp1470=
XM_005267069.3:c.4528G=	XP_005267126.2:p.Asp1510=
XM_011535984.1:c.3607G=	XP_011534286.1:p.Asp1203=
XM_011535985.1:c.3427G=	XP_011534287.1:p.Asp1143=
XM_011535986.1:c.3187G=	XP_011534288.1:p.Asp1063=
XM_011535987.1:c.2806G=	XP_011534289.1:p.Asp936=
XM_011535988.1:c.1669G=	XP_011534290.1:p.Asp557=
NM_001346813.1:c.4528G=	NP_001333742.1:p.Asp1510=
NM_001363725.1:c.2278G=	NP_001350654.1:p.Asp760=
XM_011535984.2:c.4738G=	XP_011534286.2:p.Asp1580=
XM_011535988.3:c.1669G=	XP_011534290.1:p.Asp557=
XM_017011103.2:c.4639G=	XP_016866592.1:p.Asp1547=
XM_017011104.1:c.4609G=	XP_016866593.1:p.Asp1537=
XM_017011105.2:c.4579G=	XP_016866594.1:p.Asp1527=
XM_017011106.2:c.4450G=	XP_016866595.1:p.Asp1484=
XM_017011107.2:c.4429G=	XP_016866596.1:p.Asp1477=
XR_002956289.1:n.4724G=
NM_001363725.2:c.2278G=	NP_001350654.1:p.Asp760=
NM_001371656.1:c.4657G=	NP_001358585.1:p.Asp1553=
NM_001374820.1:c.4657G=	NP_001361749.1:p.Asp1553=
NM_001374828.1:c.4777G= MANE Select	NP_001361757.1:p.Asp1593=
NM_017519.3:c.4618G=	NP_059989.3:p.Asp1540=