Canonical Allele Identifier: CA452781580

Gene: ARID1B

Linked Data

• COSMIC: COSM5564286 ; COSM5564287
• MyVariant Identifiers: chr6:g.157510913A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189779A>C , CM000668.2:g.157189779A>C	GRCh38
NC_000006.11:g.157510913A>C , CM000668.1:g.157510913A>C	GRCh37
NC_000006.10:g.157552605A>C	NCBI36
NG_032093.1:g.416850A>C
NG_032093.2:g.416850A>C
NG_066624.1:g.418754A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3898A>C	ENSP00000055163.8:p.Arg1300=
ENST00000414678.8:c.3967A>C	ENSP00000412835.3:p.Arg1323=
ENST00000637015.2:c.4186A>C	ENSP00000489729.2:p.Arg1396=
ENST00000346085.10:c.3937A>C	ENSP00000344546.5:p.Arg1313=
ENST00000350026.10:c.3649A>C	ENSP00000055163.7:p.Arg1217=
ENST00000414678.7:c.2215A>C	ENSP00000412835.2:p.Arg739=
ENST00000635849.1:c.1378A>C	ENSP00000490948.1:p.Arg460=
ENST00000635957.1:c.1012A>C	ENSP00000490385.1:p.Ser338Arg
ENST00000636930.2:c.4057A>C MANE Select	ENSP00000490491.2:p.Arg1353=
ENST00000636940.1:n.2054A>C
ENST00000637015.1:c.1425A>C
ENST00000637568.1:c.1339A>C
ENST00000637741.1:n.723A>C
ENST00000637810.1:c.1399A>C	ENSP00000489636.1:p.Arg467=
ENST00000637904.1:c.1558A>C	ENSP00000490550.1:p.Arg520=
ENST00000647938.1:c.3688A>C	ENSP00000498155.1:p.Arg1230=
ENST00000346085.9:c.3688A>C	ENSP00000344546.4:p.Arg1230=
ENST00000350026.9:c.3649A>C	ENSP00000055163.7:p.Arg1217=
ENST00000414678.6:c.2215A>C	ENSP00000412835.2:p.Arg739=
NM_017519.2:c.3649A>C	NP_059989.2:p.Arg1217=
NM_020732.3:c.3688A>C	NP_065783.3:p.Arg1230=
XM_005267069.3:c.3808A>C	XP_005267126.2:p.Arg1270=
XM_011535984.1:c.2887A>C	XP_011534286.1:p.Arg963=
XM_011535985.1:c.2707A>C	XP_011534287.1:p.Arg903=
XM_011535986.1:c.2467A>C	XP_011534288.1:p.Arg823=
XM_011535987.1:c.2086A>C	XP_011534289.1:p.Arg696=
XM_011535988.1:c.949A>C	XP_011534290.1:p.Arg317=
NM_001346813.1:c.3808A>C	NP_001333742.1:p.Arg1270=
NM_001363725.1:c.1558A>C	NP_001350654.1:p.Arg520=
XM_011535984.2:c.4018A>C	XP_011534286.2:p.Arg1340=
XM_011535988.3:c.949A>C	XP_011534290.1:p.Arg317=
XM_017011103.2:c.3919A>C	XP_016866592.1:p.Arg1307=
XM_017011104.1:c.3889A>C	XP_016866593.1:p.Arg1297=
XM_017011105.2:c.3859A>C	XP_016866594.1:p.Arg1287=
XM_017011106.2:c.3730A>C	XP_016866595.1:p.Arg1244=
XM_017011107.2:c.3709A>C	XP_016866596.1:p.Arg1237=
XR_002956289.1:n.4101A>C
NM_001363725.2:c.1558A>C	NP_001350654.1:p.Arg520=
NM_001371656.1:c.3937A>C	NP_001358585.1:p.Arg1313=
NM_001374820.1:c.3937A>C	NP_001361749.1:p.Arg1313=
NM_001374828.1:c.4057A>C MANE Select	NP_001361757.1:p.Arg1353=
NM_017519.3:c.3898A>C	NP_059989.3:p.Arg1300=