Canonical Allele Identifier: CA366234180

Gene: ARID1B

Linked Data

• COSMIC: COSM4663247 ; COSM4663248
• MyVariant Identifiers: chr6:g.157510865A>G (hg19) ; chr6:g.157189731A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189731A>G , CM000668.2:g.157189731A>G	GRCh38
NC_000006.11:g.157510865A>G , CM000668.1:g.157510865A>G	GRCh37
NC_000006.10:g.157552557A>G	NCBI36
NG_032093.1:g.416802A>G
NG_032093.2:g.416802A>G
NG_066624.1:g.418706A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3850A>G	ENSP00000055163.8:p.Thr1284Ala
ENST00000414678.8:c.3919A>G	ENSP00000412835.3:p.Thr1307Ala
ENST00000637015.2:c.4138A>G	ENSP00000489729.2:p.Thr1380Ala
ENST00000346085.10:c.3889A>G	ENSP00000344546.5:p.Thr1297Ala
ENST00000350026.10:c.3601A>G	ENSP00000055163.7:p.Thr1201Ala
ENST00000414678.7:c.2167A>G	ENSP00000412835.2:p.Thr723Ala
ENST00000635849.1:c.1330A>G	ENSP00000490948.1:p.Thr444Ala
ENST00000635957.1:c.964A>G	ENSP00000490385.1:p.Thr322Ala
ENST00000636930.2:c.4009A>G MANE Select	ENSP00000490491.2:p.Thr1337Ala
ENST00000636940.1:n.2006A>G
ENST00000637015.1:c.1377A>G
ENST00000637568.1:c.1291A>G
ENST00000637741.1:n.675A>G
ENST00000637810.1:c.1351A>G	ENSP00000489636.1:p.Thr451Ala
ENST00000637904.1:c.1510A>G	ENSP00000490550.1:p.Thr504Ala
ENST00000647938.1:c.3640A>G	ENSP00000498155.1:p.Thr1214Ala
ENST00000346085.9:c.3640A>G	ENSP00000344546.4:p.Thr1214Ala
ENST00000350026.9:c.3601A>G	ENSP00000055163.7:p.Thr1201Ala
ENST00000414678.6:c.2167A>G	ENSP00000412835.2:p.Thr723Ala
NM_017519.2:c.3601A>G	NP_059989.2:p.Thr1201Ala
NM_020732.3:c.3640A>G	NP_065783.3:p.Thr1214Ala
XM_005267069.3:c.3760A>G	XP_005267126.2:p.Thr1254Ala
XM_011535984.1:c.2839A>G	XP_011534286.1:p.Thr947Ala
XM_011535985.1:c.2659A>G	XP_011534287.1:p.Thr887Ala
XM_011535986.1:c.2419A>G	XP_011534288.1:p.Thr807Ala
XM_011535987.1:c.2038A>G	XP_011534289.1:p.Thr680Ala
XM_011535988.1:c.901A>G	XP_011534290.1:p.Thr301Ala
NM_001346813.1:c.3760A>G	NP_001333742.1:p.Thr1254Ala
NM_001363725.1:c.1510A>G	NP_001350654.1:p.Thr504Ala
XM_011535984.2:c.3970A>G	XP_011534286.2:p.Thr1324Ala
XM_011535988.3:c.901A>G	XP_011534290.1:p.Thr301Ala
XM_017011103.2:c.3871A>G	XP_016866592.1:p.Thr1291Ala
XM_017011104.1:c.3841A>G	XP_016866593.1:p.Thr1281Ala
XM_017011105.2:c.3811A>G	XP_016866594.1:p.Thr1271Ala
XM_017011106.2:c.3682A>G	XP_016866595.1:p.Thr1228Ala
XM_017011107.2:c.3661A>G	XP_016866596.1:p.Thr1221Ala
XR_002956289.1:n.4053A>G
NM_001363725.2:c.1510A>G	NP_001350654.1:p.Thr504Ala
NM_001371656.1:c.3889A>G	NP_001358585.1:p.Thr1297Ala
NM_001374820.1:c.3889A>G	NP_001361749.1:p.Thr1297Ala
NM_001374828.1:c.4009A>G MANE Select	NP_001361757.1:p.Thr1337Ala
NM_017519.3:c.3850A>G	NP_059989.3:p.Thr1284Ala