Canonical Allele Identifier: CA452781492

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510786A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189652A>G , CM000668.2:g.157189652A>G	GRCh38
NC_000006.11:g.157510786A>G , CM000668.1:g.157510786A>G	GRCh37
NC_000006.10:g.157552478A>G	NCBI36
NG_032093.1:g.416723A>G
NG_032093.2:g.416723A>G
NG_066624.1:g.418627A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3771A>G	ENSP00000055163.8:p.Gly1257=
ENST00000414678.8:c.3840A>G	ENSP00000412835.3:p.Gly1280=
ENST00000637015.2:c.4059A>G	ENSP00000489729.2:p.Gly1353=
ENST00000346085.10:c.3810A>G	ENSP00000344546.5:p.Gly1270=
ENST00000350026.10:c.3522A>G	ENSP00000055163.7:p.Gly1174=
ENST00000414678.7:c.2088A>G	ENSP00000412835.2:p.Gly696=
ENST00000635849.1:c.1251A>G	ENSP00000490948.1:p.Gly417=
ENST00000635957.1:c.885A>G	ENSP00000490385.1:p.Gly295=
ENST00000636930.2:c.3930A>G MANE Select	ENSP00000490491.2:p.Gly1310=
ENST00000636940.1:n.1927A>G
ENST00000637015.1:c.1298A>G
ENST00000637568.1:c.1212A>G
ENST00000637741.1:n.596A>G
ENST00000637810.1:c.1272A>G	ENSP00000489636.1:p.Gly424=
ENST00000637904.1:c.1431A>G	ENSP00000490550.1:p.Gly477=
ENST00000647938.1:c.3561A>G	ENSP00000498155.1:p.Gly1187=
ENST00000346085.9:c.3561A>G	ENSP00000344546.4:p.Gly1187=
ENST00000350026.9:c.3522A>G	ENSP00000055163.7:p.Gly1174=
ENST00000414678.6:c.2088A>G	ENSP00000412835.2:p.Gly696=
NM_017519.2:c.3522A>G	NP_059989.2:p.Gly1174=
NM_020732.3:c.3561A>G	NP_065783.3:p.Gly1187=
XM_005267069.3:c.3681A>G	XP_005267126.2:p.Gly1227=
XM_011535984.1:c.2760A>G	XP_011534286.1:p.Gly920=
XM_011535985.1:c.2580A>G	XP_011534287.1:p.Gly860=
XM_011535986.1:c.2340A>G	XP_011534288.1:p.Gly780=
XM_011535987.1:c.1959A>G	XP_011534289.1:p.Gly653=
XM_011535988.1:c.822A>G	XP_011534290.1:p.Gly274=
NM_001346813.1:c.3681A>G	NP_001333742.1:p.Gly1227=
NM_001363725.1:c.1431A>G	NP_001350654.1:p.Gly477=
XM_011535984.2:c.3891A>G	XP_011534286.2:p.Gly1297=
XM_011535988.3:c.822A>G	XP_011534290.1:p.Gly274=
XM_017011103.2:c.3792A>G	XP_016866592.1:p.Gly1264=
XM_017011104.1:c.3762A>G	XP_016866593.1:p.Gly1254=
XM_017011105.2:c.3732A>G	XP_016866594.1:p.Gly1244=
XM_017011106.2:c.3603A>G	XP_016866595.1:p.Gly1201=
XM_017011107.2:c.3582A>G	XP_016866596.1:p.Gly1194=
XR_002956289.1:n.3974A>G
NM_001363725.2:c.1431A>G	NP_001350654.1:p.Gly477=
NM_001371656.1:c.3810A>G	NP_001358585.1:p.Gly1270=
NM_001374820.1:c.3810A>G	NP_001361749.1:p.Gly1270=
NM_001374828.1:c.3930A>G MANE Select	NP_001361757.1:p.Gly1310=
NM_017519.3:c.3771A>G	NP_059989.3:p.Gly1257=