Canonical Allele Identifier: CA366234038

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510797G>A (hg19) ; chr6:g.157189663G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189663G>A , CM000668.2:g.157189663G>A	GRCh38
NC_000006.11:g.157510797G>A , CM000668.1:g.157510797G>A	GRCh37
NC_000006.10:g.157552489G>A	NCBI36
NG_032093.1:g.416734G>A
NG_032093.2:g.416734G>A
NG_066624.1:g.418638G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3782G>A	ENSP00000055163.8:p.Gly1261Asp
ENST00000414678.8:c.3851G>A	ENSP00000412835.3:p.Gly1284Asp
ENST00000637015.2:c.4070G>A	ENSP00000489729.2:p.Gly1357Asp
ENST00000346085.10:c.3821G>A	ENSP00000344546.5:p.Gly1274Asp
ENST00000350026.10:c.3533G>A	ENSP00000055163.7:p.Gly1178Asp
ENST00000414678.7:c.2099G>A	ENSP00000412835.2:p.Gly700Asp
ENST00000635849.1:c.1262G>A	ENSP00000490948.1:p.Gly421Asp
ENST00000635957.1:c.896G>A	ENSP00000490385.1:p.Gly299Asp
ENST00000636930.2:c.3941G>A MANE Select	ENSP00000490491.2:p.Gly1314Asp
ENST00000636940.1:n.1938G>A
ENST00000637015.1:c.1309G>A
ENST00000637568.1:c.1223G>A
ENST00000637741.1:n.607G>A
ENST00000637810.1:c.1283G>A	ENSP00000489636.1:p.Gly428Asp
ENST00000637904.1:c.1442G>A	ENSP00000490550.1:p.Gly481Asp
ENST00000647938.1:c.3572G>A	ENSP00000498155.1:p.Gly1191Asp
ENST00000346085.9:c.3572G>A	ENSP00000344546.4:p.Gly1191Asp
ENST00000350026.9:c.3533G>A	ENSP00000055163.7:p.Gly1178Asp
ENST00000414678.6:c.2099G>A	ENSP00000412835.2:p.Gly700Asp
NM_017519.2:c.3533G>A	NP_059989.2:p.Gly1178Asp
NM_020732.3:c.3572G>A	NP_065783.3:p.Gly1191Asp
XM_005267069.3:c.3692G>A	XP_005267126.2:p.Gly1231Asp
XM_011535984.1:c.2771G>A	XP_011534286.1:p.Gly924Asp
XM_011535985.1:c.2591G>A	XP_011534287.1:p.Gly864Asp
XM_011535986.1:c.2351G>A	XP_011534288.1:p.Gly784Asp
XM_011535987.1:c.1970G>A	XP_011534289.1:p.Gly657Asp
XM_011535988.1:c.833G>A	XP_011534290.1:p.Gly278Asp
NM_001346813.1:c.3692G>A	NP_001333742.1:p.Gly1231Asp
NM_001363725.1:c.1442G>A	NP_001350654.1:p.Gly481Asp
XM_011535984.2:c.3902G>A	XP_011534286.2:p.Gly1301Asp
XM_011535988.3:c.833G>A	XP_011534290.1:p.Gly278Asp
XM_017011103.2:c.3803G>A	XP_016866592.1:p.Gly1268Asp
XM_017011104.1:c.3773G>A	XP_016866593.1:p.Gly1258Asp
XM_017011105.2:c.3743G>A	XP_016866594.1:p.Gly1248Asp
XM_017011106.2:c.3614G>A	XP_016866595.1:p.Gly1205Asp
XM_017011107.2:c.3593G>A	XP_016866596.1:p.Gly1198Asp
XR_002956289.1:n.3985G>A
NM_001363725.2:c.1442G>A	NP_001350654.1:p.Gly481Asp
NM_001371656.1:c.3821G>A	NP_001358585.1:p.Gly1274Asp
NM_001374820.1:c.3821G>A	NP_001361749.1:p.Gly1274Asp
NM_001374828.1:c.3941G>A MANE Select	NP_001361757.1:p.Gly1314Asp
NM_017519.3:c.3782G>A	NP_059989.3:p.Gly1261Asp