Canonical Allele Identifier: CA1675538224

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189650G= , CM000668.2:g.157189650G=	GRCh38
NC_000006.11:g.157510784G= , CM000668.1:g.157510784G=	GRCh37
NC_000006.10:g.157552476G=	NCBI36
NG_032093.1:g.416721G=
NG_032093.2:g.416721G=
NG_066624.1:g.418625G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3769G=	ENSP00000055163.8:p.Gly1257=
ENST00000414678.8:c.3838G=	ENSP00000412835.3:p.Gly1280=
ENST00000637015.2:c.4057G=	ENSP00000489729.2:p.Gly1353=
ENST00000346085.10:c.3808G=	ENSP00000344546.5:p.Gly1270=
ENST00000350026.10:c.3520G=	ENSP00000055163.7:p.Gly1174=
ENST00000414678.7:c.2086G=	ENSP00000412835.2:p.Gly696=
ENST00000635849.1:c.1249G=	ENSP00000490948.1:p.Gly417=
ENST00000635957.1:c.883G=	ENSP00000490385.1:p.Gly295=
ENST00000636930.2:c.3928G= MANE Select	ENSP00000490491.2:p.Gly1310=
ENST00000636940.1:n.1925G=
ENST00000637015.1:c.1296G=
ENST00000637568.1:c.1210G=
ENST00000637741.1:n.594G=
ENST00000637810.1:c.1270G=	ENSP00000489636.1:p.Gly424=
ENST00000637904.1:c.1429G=	ENSP00000490550.1:p.Gly477=
ENST00000647938.1:c.3559G=	ENSP00000498155.1:p.Gly1187=
ENST00000346085.9:c.3559G=	ENSP00000344546.4:p.Gly1187=
ENST00000350026.9:c.3520G=	ENSP00000055163.7:p.Gly1174=
ENST00000414678.6:c.2086G=	ENSP00000412835.2:p.Gly696=
NM_017519.2:c.3520G=	NP_059989.2:p.Gly1174=
NM_020732.3:c.3559G=	NP_065783.3:p.Gly1187=
XM_005267069.3:c.3679G=	XP_005267126.2:p.Gly1227=
XM_011535984.1:c.2758G=	XP_011534286.1:p.Gly920=
XM_011535985.1:c.2578G=	XP_011534287.1:p.Gly860=
XM_011535986.1:c.2338G=	XP_011534288.1:p.Gly780=
XM_011535987.1:c.1957G=	XP_011534289.1:p.Gly653=
XM_011535988.1:c.820G=	XP_011534290.1:p.Gly274=
NM_001346813.1:c.3679G=	NP_001333742.1:p.Gly1227=
NM_001363725.1:c.1429G=	NP_001350654.1:p.Gly477=
XM_011535984.2:c.3889G=	XP_011534286.2:p.Gly1297=
XM_011535988.3:c.820G=	XP_011534290.1:p.Gly274=
XM_017011103.2:c.3790G=	XP_016866592.1:p.Gly1264=
XM_017011104.1:c.3760G=	XP_016866593.1:p.Gly1254=
XM_017011105.2:c.3730G=	XP_016866594.1:p.Gly1244=
XM_017011106.2:c.3601G=	XP_016866595.1:p.Gly1201=
XM_017011107.2:c.3580G=	XP_016866596.1:p.Gly1194=
XR_002956289.1:n.3972G=
NM_001363725.2:c.1429G=	NP_001350654.1:p.Gly477=
NM_001371656.1:c.3808G=	NP_001358585.1:p.Gly1270=
NM_001374820.1:c.3808G=	NP_001361749.1:p.Gly1270=
NM_001374828.1:c.3928G= MANE Select	NP_001361757.1:p.Gly1310=
NM_017519.3:c.3769G=	NP_059989.3:p.Gly1257=