Canonical Allele Identifier: CA366235325

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511260T>G (hg19) ; chr6:g.157190126T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190126T>G , CM000668.2:g.157190126T>G	GRCh38
NC_000006.11:g.157511260T>G , CM000668.1:g.157511260T>G	GRCh37
NC_000006.10:g.157552952T>G	NCBI36
NG_032093.1:g.417197T>G
NG_032093.2:g.417197T>G
NG_066624.1:g.419101T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3988T>G	ENSP00000055163.8:p.Tyr1330Asp
ENST00000414678.8:c.4057T>G	ENSP00000412835.3:p.Tyr1353Asp
ENST00000637015.2:c.4276T>G	ENSP00000489729.2:p.Tyr1426Asp
ENST00000346085.10:c.4027T>G	ENSP00000344546.5:p.Tyr1343Asp
ENST00000350026.10:c.3739T>G	ENSP00000055163.7:p.Tyr1247Asp
ENST00000414678.7:c.2305T>G	ENSP00000412835.2:p.Tyr769Asp
ENST00000635849.1:c.1468T>G	ENSP00000490948.1:p.Tyr490Asp
ENST00000635957.1:c.1099T>G	ENSP00000490385.1:p.Tyr367Asp
ENST00000636930.2:c.4147T>G MANE Select	ENSP00000490491.2:p.Tyr1383Asp
ENST00000636940.1:n.2144T>G
ENST00000637015.1:c.1515T>G
ENST00000637568.1:c.1429T>G
ENST00000637741.1:n.813T>G
ENST00000637810.1:c.1489T>G	ENSP00000489636.1:p.Tyr497Asp
ENST00000637904.1:c.1648T>G	ENSP00000490550.1:p.Tyr550Asp
ENST00000647938.1:c.3778T>G	ENSP00000498155.1:p.Tyr1260Asp
ENST00000346085.9:c.3778T>G	ENSP00000344546.4:p.Tyr1260Asp
ENST00000350026.9:c.3739T>G	ENSP00000055163.7:p.Tyr1247Asp
ENST00000414678.6:c.2305T>G	ENSP00000412835.2:p.Tyr769Asp
NM_017519.2:c.3739T>G	NP_059989.2:p.Tyr1247Asp
NM_020732.3:c.3778T>G	NP_065783.3:p.Tyr1260Asp
XM_005267069.3:c.3898T>G	XP_005267126.2:p.Tyr1300Asp
XM_011535984.1:c.2977T>G	XP_011534286.1:p.Tyr993Asp
XM_011535985.1:c.2797T>G	XP_011534287.1:p.Tyr933Asp
XM_011535986.1:c.2557T>G	XP_011534288.1:p.Tyr853Asp
XM_011535987.1:c.2176T>G	XP_011534289.1:p.Tyr726Asp
XM_011535988.1:c.1039T>G	XP_011534290.1:p.Tyr347Asp
NM_001346813.1:c.3898T>G	NP_001333742.1:p.Tyr1300Asp
NM_001363725.1:c.1648T>G	NP_001350654.1:p.Tyr550Asp
XM_011535984.2:c.4108T>G	XP_011534286.2:p.Tyr1370Asp
XM_011535988.3:c.1039T>G	XP_011534290.1:p.Tyr347Asp
XM_017011103.2:c.4009T>G	XP_016866592.1:p.Tyr1337Asp
XM_017011104.1:c.3979T>G	XP_016866593.1:p.Tyr1327Asp
XM_017011105.2:c.3949T>G	XP_016866594.1:p.Tyr1317Asp
XM_017011106.2:c.3820T>G	XP_016866595.1:p.Tyr1274Asp
XM_017011107.2:c.3799T>G	XP_016866596.1:p.Tyr1267Asp
XR_002956289.1:n.4191T>G
NM_001363725.2:c.1648T>G	NP_001350654.1:p.Tyr550Asp
NM_001371656.1:c.4027T>G	NP_001358585.1:p.Tyr1343Asp
NM_001374820.1:c.4027T>G	NP_001361749.1:p.Tyr1343Asp
NM_001374828.1:c.4147T>G MANE Select	NP_001361757.1:p.Tyr1383Asp
NM_017519.3:c.3988T>G	NP_059989.3:p.Tyr1330Asp