Canonical Allele Identifier: CA366241887

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522217G>T (hg19) ; chr6:g.157201083G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201083G>T , CM000668.2:g.157201083G>T	GRCh38
NC_000006.11:g.157522217G>T , CM000668.1:g.157522217G>T	GRCh37
NC_000006.10:g.157563909G>T	NCBI36
NG_032093.1:g.428154G>T
NG_032093.2:g.428154G>T
NG_066624.1:g.430058G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4699G>T	ENSP00000055163.8:p.Asp1567Tyr
ENST00000414678.8:c.4768G>T	ENSP00000412835.3:p.Asp1590Tyr
ENST00000637015.2:c.4987G>T	ENSP00000489729.2:p.Asp1663Tyr
ENST00000346085.10:c.4738G>T	ENSP00000344546.5:p.Asp1580Tyr
ENST00000350026.10:c.4450G>T	ENSP00000055163.7:p.Asp1484Tyr
ENST00000414678.7:c.3016G>T	ENSP00000412835.2:p.Asp1006Tyr
ENST00000635849.1:c.2179G>T	ENSP00000490948.1:p.Asp727Tyr
ENST00000635957.1:c.1810G>T	ENSP00000490385.1:p.Asp604Tyr
ENST00000636227.1:n.3321G>T
ENST00000636254.1:n.778G>T
ENST00000636930.2:c.4858G>T MANE Select	ENSP00000490491.2:p.Asp1620Tyr
ENST00000636940.1:n.2855G>T
ENST00000637015.1:c.2226G>T
ENST00000637568.1:c.2140G>T
ENST00000637741.1:n.1524G>T
ENST00000637810.1:c.2200G>T	ENSP00000489636.1:p.Asp734Tyr
ENST00000637904.1:c.2359G>T	ENSP00000490550.1:p.Asp787Tyr
ENST00000647938.1:c.4489G>T	ENSP00000498155.1:p.Asp1497Tyr
ENST00000346085.9:c.4489G>T	ENSP00000344546.4:p.Asp1497Tyr
ENST00000350026.9:c.4450G>T	ENSP00000055163.7:p.Asp1484Tyr
ENST00000414678.6:c.3016G>T	ENSP00000412835.2:p.Asp1006Tyr
NM_017519.2:c.4450G>T	NP_059989.2:p.Asp1484Tyr
NM_020732.3:c.4489G>T	NP_065783.3:p.Asp1497Tyr
XM_005267069.3:c.4609G>T	XP_005267126.2:p.Asp1537Tyr
XM_011535984.1:c.3688G>T	XP_011534286.1:p.Asp1230Tyr
XM_011535985.1:c.3508G>T	XP_011534287.1:p.Asp1170Tyr
XM_011535986.1:c.3268G>T	XP_011534288.1:p.Asp1090Tyr
XM_011535987.1:c.2887G>T	XP_011534289.1:p.Asp963Tyr
XM_011535988.1:c.1750G>T	XP_011534290.1:p.Asp584Tyr
NM_001346813.1:c.4609G>T	NP_001333742.1:p.Asp1537Tyr
NM_001363725.1:c.2359G>T	NP_001350654.1:p.Asp787Tyr
XM_011535984.2:c.4819G>T	XP_011534286.2:p.Asp1607Tyr
XM_011535988.3:c.1750G>T	XP_011534290.1:p.Asp584Tyr
XM_017011103.2:c.4720G>T	XP_016866592.1:p.Asp1574Tyr
XM_017011104.1:c.4690G>T	XP_016866593.1:p.Asp1564Tyr
XM_017011105.2:c.4660G>T	XP_016866594.1:p.Asp1554Tyr
XM_017011106.2:c.4531G>T	XP_016866595.1:p.Asp1511Tyr
XM_017011107.2:c.4510G>T	XP_016866596.1:p.Asp1504Tyr
XR_002956289.1:n.4805G>T
NM_001363725.2:c.2359G>T	NP_001350654.1:p.Asp787Tyr
NM_001371656.1:c.4738G>T	NP_001358585.1:p.Asp1580Tyr
NM_001374820.1:c.4738G>T	NP_001361749.1:p.Asp1580Tyr
NM_001374828.1:c.4858G>T MANE Select	NP_001361757.1:p.Asp1620Tyr
NM_017519.3:c.4699G>T	NP_059989.3:p.Asp1567Tyr