Canonical Allele Identifier: CA366234207

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510878C>G (hg19) ; chr6:g.157189744C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189744C>G , CM000668.2:g.157189744C>G	GRCh38
NC_000006.11:g.157510878C>G , CM000668.1:g.157510878C>G	GRCh37
NC_000006.10:g.157552570C>G	NCBI36
NG_032093.1:g.416815C>G
NG_032093.2:g.416815C>G
NG_066624.1:g.418719C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3863C>G	ENSP00000055163.8:p.Thr1288Ser
ENST00000414678.8:c.3932C>G	ENSP00000412835.3:p.Thr1311Ser
ENST00000637015.2:c.4151C>G	ENSP00000489729.2:p.Thr1384Ser
ENST00000346085.10:c.3902C>G	ENSP00000344546.5:p.Thr1301Ser
ENST00000350026.10:c.3614C>G	ENSP00000055163.7:p.Thr1205Ser
ENST00000414678.7:c.2180C>G	ENSP00000412835.2:p.Thr727Ser
ENST00000635849.1:c.1343C>G	ENSP00000490948.1:p.Thr448Ser
ENST00000635957.1:c.977C>G	ENSP00000490385.1:p.Thr326Ser
ENST00000636930.2:c.4022C>G MANE Select	ENSP00000490491.2:p.Thr1341Ser
ENST00000636940.1:n.2019C>G
ENST00000637015.1:c.1390C>G
ENST00000637568.1:c.1304C>G
ENST00000637741.1:n.688C>G
ENST00000637810.1:c.1364C>G	ENSP00000489636.1:p.Thr455Ser
ENST00000637904.1:c.1523C>G	ENSP00000490550.1:p.Thr508Ser
ENST00000647938.1:c.3653C>G	ENSP00000498155.1:p.Thr1218Ser
ENST00000346085.9:c.3653C>G	ENSP00000344546.4:p.Thr1218Ser
ENST00000350026.9:c.3614C>G	ENSP00000055163.7:p.Thr1205Ser
ENST00000414678.6:c.2180C>G	ENSP00000412835.2:p.Thr727Ser
NM_017519.2:c.3614C>G	NP_059989.2:p.Thr1205Ser
NM_020732.3:c.3653C>G	NP_065783.3:p.Thr1218Ser
XM_005267069.3:c.3773C>G	XP_005267126.2:p.Thr1258Ser
XM_011535984.1:c.2852C>G	XP_011534286.1:p.Thr951Ser
XM_011535985.1:c.2672C>G	XP_011534287.1:p.Thr891Ser
XM_011535986.1:c.2432C>G	XP_011534288.1:p.Thr811Ser
XM_011535987.1:c.2051C>G	XP_011534289.1:p.Thr684Ser
XM_011535988.1:c.914C>G	XP_011534290.1:p.Thr305Ser
NM_001346813.1:c.3773C>G	NP_001333742.1:p.Thr1258Ser
NM_001363725.1:c.1523C>G	NP_001350654.1:p.Thr508Ser
XM_011535984.2:c.3983C>G	XP_011534286.2:p.Thr1328Ser
XM_011535988.3:c.914C>G	XP_011534290.1:p.Thr305Ser
XM_017011103.2:c.3884C>G	XP_016866592.1:p.Thr1295Ser
XM_017011104.1:c.3854C>G	XP_016866593.1:p.Thr1285Ser
XM_017011105.2:c.3824C>G	XP_016866594.1:p.Thr1275Ser
XM_017011106.2:c.3695C>G	XP_016866595.1:p.Thr1232Ser
XM_017011107.2:c.3674C>G	XP_016866596.1:p.Thr1225Ser
XR_002956289.1:n.4066C>G
NM_001363725.2:c.1523C>G	NP_001350654.1:p.Thr508Ser
NM_001371656.1:c.3902C>G	NP_001358585.1:p.Thr1301Ser
NM_001374820.1:c.3902C>G	NP_001361749.1:p.Thr1301Ser
NM_001374828.1:c.4022C>G MANE Select	NP_001361757.1:p.Thr1341Ser
NM_017519.3:c.3863C>G	NP_059989.3:p.Thr1288Ser