Canonical Allele Identifier: CA452781560

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510879C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189745C>G , CM000668.2:g.157189745C>G	GRCh38
NC_000006.11:g.157510879C>G , CM000668.1:g.157510879C>G	GRCh37
NC_000006.10:g.157552571C>G	NCBI36
NG_032093.1:g.416816C>G
NG_032093.2:g.416816C>G
NG_066624.1:g.418720C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3864C>G	ENSP00000055163.8:p.Thr1288=
ENST00000414678.8:c.3933C>G	ENSP00000412835.3:p.Thr1311=
ENST00000637015.2:c.4152C>G	ENSP00000489729.2:p.Thr1384=
ENST00000346085.10:c.3903C>G	ENSP00000344546.5:p.Thr1301=
ENST00000350026.10:c.3615C>G	ENSP00000055163.7:p.Thr1205=
ENST00000414678.7:c.2181C>G	ENSP00000412835.2:p.Thr727=
ENST00000635849.1:c.1344C>G	ENSP00000490948.1:p.Thr448=
ENST00000635957.1:c.978C>G	ENSP00000490385.1:p.Thr326=
ENST00000636930.2:c.4023C>G MANE Select	ENSP00000490491.2:p.Thr1341=
ENST00000636940.1:n.2020C>G
ENST00000637015.1:c.1391C>G
ENST00000637568.1:c.1305C>G
ENST00000637741.1:n.689C>G
ENST00000637810.1:c.1365C>G	ENSP00000489636.1:p.Thr455=
ENST00000637904.1:c.1524C>G	ENSP00000490550.1:p.Thr508=
ENST00000647938.1:c.3654C>G	ENSP00000498155.1:p.Thr1218=
ENST00000346085.9:c.3654C>G	ENSP00000344546.4:p.Thr1218=
ENST00000350026.9:c.3615C>G	ENSP00000055163.7:p.Thr1205=
ENST00000414678.6:c.2181C>G	ENSP00000412835.2:p.Thr727=
NM_017519.2:c.3615C>G	NP_059989.2:p.Thr1205=
NM_020732.3:c.3654C>G	NP_065783.3:p.Thr1218=
XM_005267069.3:c.3774C>G	XP_005267126.2:p.Thr1258=
XM_011535984.1:c.2853C>G	XP_011534286.1:p.Thr951=
XM_011535985.1:c.2673C>G	XP_011534287.1:p.Thr891=
XM_011535986.1:c.2433C>G	XP_011534288.1:p.Thr811=
XM_011535987.1:c.2052C>G	XP_011534289.1:p.Thr684=
XM_011535988.1:c.915C>G	XP_011534290.1:p.Thr305=
NM_001346813.1:c.3774C>G	NP_001333742.1:p.Thr1258=
NM_001363725.1:c.1524C>G	NP_001350654.1:p.Thr508=
XM_011535984.2:c.3984C>G	XP_011534286.2:p.Thr1328=
XM_011535988.3:c.915C>G	XP_011534290.1:p.Thr305=
XM_017011103.2:c.3885C>G	XP_016866592.1:p.Thr1295=
XM_017011104.1:c.3855C>G	XP_016866593.1:p.Thr1285=
XM_017011105.2:c.3825C>G	XP_016866594.1:p.Thr1275=
XM_017011106.2:c.3696C>G	XP_016866595.1:p.Thr1232=
XM_017011107.2:c.3675C>G	XP_016866596.1:p.Thr1225=
XR_002956289.1:n.4067C>G
NM_001363725.2:c.1524C>G	NP_001350654.1:p.Thr508=
NM_001371656.1:c.3903C>G	NP_001358585.1:p.Thr1301=
NM_001374820.1:c.3903C>G	NP_001361749.1:p.Thr1301=
NM_001374828.1:c.4023C>G MANE Select	NP_001361757.1:p.Thr1341=
NM_017519.3:c.3864C>G	NP_059989.3:p.Thr1288=