Canonical Allele Identifier: CA366235323

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3988T>A	ENSP00000055163.8:p.Tyr1330Asn
ENST00000414678.8:c.4057T>A	ENSP00000412835.3:p.Tyr1353Asn
ENST00000637015.2:c.4276T>A	ENSP00000489729.2:p.Tyr1426Asn
ENST00000346085.10:c.4027T>A	ENSP00000344546.5:p.Tyr1343Asn
ENST00000350026.10:c.3739T>A	ENSP00000055163.7:p.Tyr1247Asn
ENST00000414678.7:c.2305T>A	ENSP00000412835.2:p.Tyr769Asn
ENST00000635849.1:c.1468T>A	ENSP00000490948.1:p.Tyr490Asn
ENST00000635957.1:c.1099T>A	ENSP00000490385.1:p.Tyr367Asn
ENST00000636930.2:c.4147T>A MANE Select	ENSP00000490491.2:p.Tyr1383Asn
ENST00000636940.1:n.2144T>A
ENST00000637015.1:c.1515T>A
ENST00000637568.1:c.1429T>A
ENST00000637741.1:n.813T>A
ENST00000637810.1:c.1489T>A	ENSP00000489636.1:p.Tyr497Asn
ENST00000637904.1:c.1648T>A	ENSP00000490550.1:p.Tyr550Asn
ENST00000647938.1:c.3778T>A	ENSP00000498155.1:p.Tyr1260Asn
ENST00000346085.9:c.3778T>A	ENSP00000344546.4:p.Tyr1260Asn
ENST00000350026.9:c.3739T>A	ENSP00000055163.7:p.Tyr1247Asn
ENST00000414678.6:c.2305T>A	ENSP00000412835.2:p.Tyr769Asn
NM_017519.2:c.3739T>A	NP_059989.2:p.Tyr1247Asn
NM_020732.3:c.3778T>A	NP_065783.3:p.Tyr1260Asn
XM_005267069.3:c.3898T>A	XP_005267126.2:p.Tyr1300Asn
XM_011535984.1:c.2977T>A	XP_011534286.1:p.Tyr993Asn
XM_011535985.1:c.2797T>A	XP_011534287.1:p.Tyr933Asn
XM_011535986.1:c.2557T>A	XP_011534288.1:p.Tyr853Asn
XM_011535987.1:c.2176T>A	XP_011534289.1:p.Tyr726Asn
XM_011535988.1:c.1039T>A	XP_011534290.1:p.Tyr347Asn
NM_001346813.1:c.3898T>A	NP_001333742.1:p.Tyr1300Asn
NM_001363725.1:c.1648T>A	NP_001350654.1:p.Tyr550Asn
XM_011535984.2:c.4108T>A	XP_011534286.2:p.Tyr1370Asn
XM_011535988.3:c.1039T>A	XP_011534290.1:p.Tyr347Asn
XM_017011103.2:c.4009T>A	XP_016866592.1:p.Tyr1337Asn
XM_017011104.1:c.3979T>A	XP_016866593.1:p.Tyr1327Asn
XM_017011105.2:c.3949T>A	XP_016866594.1:p.Tyr1317Asn
XM_017011106.2:c.3820T>A	XP_016866595.1:p.Tyr1274Asn
XM_017011107.2:c.3799T>A	XP_016866596.1:p.Tyr1267Asn
XR_002956289.1:n.4191T>A
NM_001363725.2:c.1648T>A	NP_001350654.1:p.Tyr550Asn
NM_001371656.1:c.4027T>A	NP_001358585.1:p.Tyr1343Asn
NM_001374820.1:c.4027T>A	NP_001361749.1:p.Tyr1343Asn
NM_001374828.1:c.4147T>A MANE Select	NP_001361757.1:p.Tyr1383Asn
NM_017519.3:c.3988T>A	NP_059989.3:p.Tyr1330Asn