Canonical Allele Identifier: CA366234437

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510913A>G (hg19) ; chr6:g.157189779A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189779A>G , CM000668.2:g.157189779A>G	GRCh38
NC_000006.11:g.157510913A>G , CM000668.1:g.157510913A>G	GRCh37
NC_000006.10:g.157552605A>G	NCBI36
NG_032093.1:g.416850A>G
NG_032093.2:g.416850A>G
NG_066624.1:g.418754A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3898A>G	ENSP00000055163.8:p.Arg1300Gly
ENST00000414678.8:c.3967A>G	ENSP00000412835.3:p.Arg1323Gly
ENST00000637015.2:c.4186A>G	ENSP00000489729.2:p.Arg1396Gly
ENST00000346085.10:c.3937A>G	ENSP00000344546.5:p.Arg1313Gly
ENST00000350026.10:c.3649A>G	ENSP00000055163.7:p.Arg1217Gly
ENST00000414678.7:c.2215A>G	ENSP00000412835.2:p.Arg739Gly
ENST00000635849.1:c.1378A>G	ENSP00000490948.1:p.Arg460Gly
ENST00000635957.1:c.1012A>G	ENSP00000490385.1:p.Ser338Gly
ENST00000636930.2:c.4057A>G MANE Select	ENSP00000490491.2:p.Arg1353Gly
ENST00000636940.1:n.2054A>G
ENST00000637015.1:c.1425A>G
ENST00000637568.1:c.1339A>G
ENST00000637741.1:n.723A>G
ENST00000637810.1:c.1399A>G	ENSP00000489636.1:p.Arg467Gly
ENST00000637904.1:c.1558A>G	ENSP00000490550.1:p.Arg520Gly
ENST00000647938.1:c.3688A>G	ENSP00000498155.1:p.Arg1230Gly
ENST00000346085.9:c.3688A>G	ENSP00000344546.4:p.Arg1230Gly
ENST00000350026.9:c.3649A>G	ENSP00000055163.7:p.Arg1217Gly
ENST00000414678.6:c.2215A>G	ENSP00000412835.2:p.Arg739Gly
NM_017519.2:c.3649A>G	NP_059989.2:p.Arg1217Gly
NM_020732.3:c.3688A>G	NP_065783.3:p.Arg1230Gly
XM_005267069.3:c.3808A>G	XP_005267126.2:p.Arg1270Gly
XM_011535984.1:c.2887A>G	XP_011534286.1:p.Arg963Gly
XM_011535985.1:c.2707A>G	XP_011534287.1:p.Arg903Gly
XM_011535986.1:c.2467A>G	XP_011534288.1:p.Arg823Gly
XM_011535987.1:c.2086A>G	XP_011534289.1:p.Arg696Gly
XM_011535988.1:c.949A>G	XP_011534290.1:p.Arg317Gly
NM_001346813.1:c.3808A>G	NP_001333742.1:p.Arg1270Gly
NM_001363725.1:c.1558A>G	NP_001350654.1:p.Arg520Gly
XM_011535984.2:c.4018A>G	XP_011534286.2:p.Arg1340Gly
XM_011535988.3:c.949A>G	XP_011534290.1:p.Arg317Gly
XM_017011103.2:c.3919A>G	XP_016866592.1:p.Arg1307Gly
XM_017011104.1:c.3889A>G	XP_016866593.1:p.Arg1297Gly
XM_017011105.2:c.3859A>G	XP_016866594.1:p.Arg1287Gly
XM_017011106.2:c.3730A>G	XP_016866595.1:p.Arg1244Gly
XM_017011107.2:c.3709A>G	XP_016866596.1:p.Arg1237Gly
XR_002956289.1:n.4101A>G
NM_001363725.2:c.1558A>G	NP_001350654.1:p.Arg520Gly
NM_001371656.1:c.3937A>G	NP_001358585.1:p.Arg1313Gly
NM_001374820.1:c.3937A>G	NP_001361749.1:p.Arg1313Gly
NM_001374828.1:c.4057A>G MANE Select	NP_001361757.1:p.Arg1353Gly
NM_017519.3:c.3898A>G	NP_059989.3:p.Arg1300Gly