Canonical Allele Identifier: CA366234040

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3782G>T	ENSP00000055163.8:p.Gly1261Val
ENST00000414678.8:c.3851G>T	ENSP00000412835.3:p.Gly1284Val
ENST00000637015.2:c.4070G>T	ENSP00000489729.2:p.Gly1357Val
ENST00000346085.10:c.3821G>T	ENSP00000344546.5:p.Gly1274Val
ENST00000350026.10:c.3533G>T	ENSP00000055163.7:p.Gly1178Val
ENST00000414678.7:c.2099G>T	ENSP00000412835.2:p.Gly700Val
ENST00000635849.1:c.1262G>T	ENSP00000490948.1:p.Gly421Val
ENST00000635957.1:c.896G>T	ENSP00000490385.1:p.Gly299Val
ENST00000636930.2:c.3941G>T MANE Select	ENSP00000490491.2:p.Gly1314Val
ENST00000636940.1:n.1938G>T
ENST00000637015.1:c.1309G>T
ENST00000637568.1:c.1223G>T
ENST00000637741.1:n.607G>T
ENST00000637810.1:c.1283G>T	ENSP00000489636.1:p.Gly428Val
ENST00000637904.1:c.1442G>T	ENSP00000490550.1:p.Gly481Val
ENST00000647938.1:c.3572G>T	ENSP00000498155.1:p.Gly1191Val
ENST00000346085.9:c.3572G>T	ENSP00000344546.4:p.Gly1191Val
ENST00000350026.9:c.3533G>T	ENSP00000055163.7:p.Gly1178Val
ENST00000414678.6:c.2099G>T	ENSP00000412835.2:p.Gly700Val
NM_017519.2:c.3533G>T	NP_059989.2:p.Gly1178Val
NM_020732.3:c.3572G>T	NP_065783.3:p.Gly1191Val
XM_005267069.3:c.3692G>T	XP_005267126.2:p.Gly1231Val
XM_011535984.1:c.2771G>T	XP_011534286.1:p.Gly924Val
XM_011535985.1:c.2591G>T	XP_011534287.1:p.Gly864Val
XM_011535986.1:c.2351G>T	XP_011534288.1:p.Gly784Val
XM_011535987.1:c.1970G>T	XP_011534289.1:p.Gly657Val
XM_011535988.1:c.833G>T	XP_011534290.1:p.Gly278Val
NM_001346813.1:c.3692G>T	NP_001333742.1:p.Gly1231Val
NM_001363725.1:c.1442G>T	NP_001350654.1:p.Gly481Val
XM_011535984.2:c.3902G>T	XP_011534286.2:p.Gly1301Val
XM_011535988.3:c.833G>T	XP_011534290.1:p.Gly278Val
XM_017011103.2:c.3803G>T	XP_016866592.1:p.Gly1268Val
XM_017011104.1:c.3773G>T	XP_016866593.1:p.Gly1258Val
XM_017011105.2:c.3743G>T	XP_016866594.1:p.Gly1248Val
XM_017011106.2:c.3614G>T	XP_016866595.1:p.Gly1205Val
XM_017011107.2:c.3593G>T	XP_016866596.1:p.Gly1198Val
XR_002956289.1:n.3985G>T
NM_001363725.2:c.1442G>T	NP_001350654.1:p.Gly481Val
NM_001371656.1:c.3821G>T	NP_001358585.1:p.Gly1274Val
NM_001374820.1:c.3821G>T	NP_001361749.1:p.Gly1274Val
NM_001374828.1:c.3941G>T MANE Select	NP_001361757.1:p.Gly1314Val
NM_017519.3:c.3782G>T	NP_059989.3:p.Gly1261Val