Canonical Allele Identifier: CA366234202

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510877A>G (hg19) ; chr6:g.157189743A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189743A>G , CM000668.2:g.157189743A>G	GRCh38
NC_000006.11:g.157510877A>G , CM000668.1:g.157510877A>G	GRCh37
NC_000006.10:g.157552569A>G	NCBI36
NG_032093.1:g.416814A>G
NG_032093.2:g.416814A>G
NG_066624.1:g.418718A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3862A>G	ENSP00000055163.8:p.Thr1288Ala
ENST00000414678.8:c.3931A>G	ENSP00000412835.3:p.Thr1311Ala
ENST00000637015.2:c.4150A>G	ENSP00000489729.2:p.Thr1384Ala
ENST00000346085.10:c.3901A>G	ENSP00000344546.5:p.Thr1301Ala
ENST00000350026.10:c.3613A>G	ENSP00000055163.7:p.Thr1205Ala
ENST00000414678.7:c.2179A>G	ENSP00000412835.2:p.Thr727Ala
ENST00000635849.1:c.1342A>G	ENSP00000490948.1:p.Thr448Ala
ENST00000635957.1:c.976A>G	ENSP00000490385.1:p.Thr326Ala
ENST00000636930.2:c.4021A>G MANE Select	ENSP00000490491.2:p.Thr1341Ala
ENST00000636940.1:n.2018A>G
ENST00000637015.1:c.1389A>G
ENST00000637568.1:c.1303A>G
ENST00000637741.1:n.687A>G
ENST00000637810.1:c.1363A>G	ENSP00000489636.1:p.Thr455Ala
ENST00000637904.1:c.1522A>G	ENSP00000490550.1:p.Thr508Ala
ENST00000647938.1:c.3652A>G	ENSP00000498155.1:p.Thr1218Ala
ENST00000346085.9:c.3652A>G	ENSP00000344546.4:p.Thr1218Ala
ENST00000350026.9:c.3613A>G	ENSP00000055163.7:p.Thr1205Ala
ENST00000414678.6:c.2179A>G	ENSP00000412835.2:p.Thr727Ala
NM_017519.2:c.3613A>G	NP_059989.2:p.Thr1205Ala
NM_020732.3:c.3652A>G	NP_065783.3:p.Thr1218Ala
XM_005267069.3:c.3772A>G	XP_005267126.2:p.Thr1258Ala
XM_011535984.1:c.2851A>G	XP_011534286.1:p.Thr951Ala
XM_011535985.1:c.2671A>G	XP_011534287.1:p.Thr891Ala
XM_011535986.1:c.2431A>G	XP_011534288.1:p.Thr811Ala
XM_011535987.1:c.2050A>G	XP_011534289.1:p.Thr684Ala
XM_011535988.1:c.913A>G	XP_011534290.1:p.Thr305Ala
NM_001346813.1:c.3772A>G	NP_001333742.1:p.Thr1258Ala
NM_001363725.1:c.1522A>G	NP_001350654.1:p.Thr508Ala
XM_011535984.2:c.3982A>G	XP_011534286.2:p.Thr1328Ala
XM_011535988.3:c.913A>G	XP_011534290.1:p.Thr305Ala
XM_017011103.2:c.3883A>G	XP_016866592.1:p.Thr1295Ala
XM_017011104.1:c.3853A>G	XP_016866593.1:p.Thr1285Ala
XM_017011105.2:c.3823A>G	XP_016866594.1:p.Thr1275Ala
XM_017011106.2:c.3694A>G	XP_016866595.1:p.Thr1232Ala
XM_017011107.2:c.3673A>G	XP_016866596.1:p.Thr1225Ala
XR_002956289.1:n.4065A>G
NM_001363725.2:c.1522A>G	NP_001350654.1:p.Thr508Ala
NM_001371656.1:c.3901A>G	NP_001358585.1:p.Thr1301Ala
NM_001374820.1:c.3901A>G	NP_001361749.1:p.Thr1301Ala
NM_001374828.1:c.4021A>G MANE Select	NP_001361757.1:p.Thr1341Ala
NM_017519.3:c.3862A>G	NP_059989.3:p.Thr1288Ala