Canonical Allele Identifier: CA366242689

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376135
• MyVariant Identifiers: chr6:g.157522484A>T (hg19) ; chr6:g.157201350A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201350A>T , CM000668.2:g.157201350A>T	GRCh38
NC_000006.11:g.157522484A>T , CM000668.1:g.157522484A>T	GRCh37
NC_000006.10:g.157564176A>T	NCBI36
NG_032093.1:g.428421A>T
NG_032093.2:g.428421A>T
NG_066624.1:g.430325A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4966A>T	ENSP00000055163.8:p.Thr1656Ser
ENST00000414678.8:c.5035A>T	ENSP00000412835.3:p.Thr1679Ser
ENST00000637015.2:c.5254A>T	ENSP00000489729.2:p.Thr1752Ser
ENST00000346085.10:c.5005A>T	ENSP00000344546.5:p.Thr1669Ser
ENST00000350026.10:c.4717A>T	ENSP00000055163.7:p.Thr1573Ser
ENST00000414678.7:c.3283A>T	ENSP00000412835.2:p.Thr1095Ser
ENST00000635849.1:c.2446A>T	ENSP00000490948.1:p.Thr816Ser
ENST00000635957.1:c.2077A>T	ENSP00000490385.1:p.Thr693Ser
ENST00000636227.1:n.3588A>T
ENST00000636254.1:n.1045A>T
ENST00000636930.2:c.5125A>T MANE Select	ENSP00000490491.2:p.Thr1709Ser
ENST00000636940.1:n.3122A>T
ENST00000637015.1:c.2493A>T
ENST00000637568.1:c.2407A>T
ENST00000637741.1:n.1791A>T
ENST00000637810.1:c.2467A>T	ENSP00000489636.1:p.Thr823Ser
ENST00000637904.1:c.2626A>T	ENSP00000490550.1:p.Thr876Ser
ENST00000647938.1:c.4756A>T	ENSP00000498155.1:p.Thr1586Ser
ENST00000346085.9:c.4756A>T	ENSP00000344546.4:p.Thr1586Ser
ENST00000350026.9:c.4717A>T	ENSP00000055163.7:p.Thr1573Ser
ENST00000414678.6:c.3283A>T	ENSP00000412835.2:p.Thr1095Ser
NM_017519.2:c.4717A>T	NP_059989.2:p.Thr1573Ser
NM_020732.3:c.4756A>T	NP_065783.3:p.Thr1586Ser
XM_005267069.3:c.4876A>T	XP_005267126.2:p.Thr1626Ser
XM_011535984.1:c.3955A>T	XP_011534286.1:p.Thr1319Ser
XM_011535985.1:c.3775A>T	XP_011534287.1:p.Thr1259Ser
XM_011535986.1:c.3535A>T	XP_011534288.1:p.Thr1179Ser
XM_011535987.1:c.3154A>T	XP_011534289.1:p.Thr1052Ser
XM_011535988.1:c.2017A>T	XP_011534290.1:p.Thr673Ser
NM_001346813.1:c.4876A>T	NP_001333742.1:p.Thr1626Ser
NM_001363725.1:c.2626A>T	NP_001350654.1:p.Thr876Ser
XM_011535984.2:c.5086A>T	XP_011534286.2:p.Thr1696Ser
XM_011535988.3:c.2017A>T	XP_011534290.1:p.Thr673Ser
XM_017011103.2:c.4987A>T	XP_016866592.1:p.Thr1663Ser
XM_017011104.1:c.4957A>T	XP_016866593.1:p.Thr1653Ser
XM_017011105.2:c.4927A>T	XP_016866594.1:p.Thr1643Ser
XM_017011106.2:c.4798A>T	XP_016866595.1:p.Thr1600Ser
XM_017011107.2:c.4777A>T	XP_016866596.1:p.Thr1593Ser
XR_002956289.1:n.5072A>T
NM_001363725.2:c.2626A>T	NP_001350654.1:p.Thr876Ser
NM_001371656.1:c.5005A>T	NP_001358585.1:p.Thr1669Ser
NM_001374820.1:c.5005A>T	NP_001361749.1:p.Thr1669Ser
NM_001374828.1:c.5125A>T MANE Select	NP_001361757.1:p.Thr1709Ser
NM_017519.3:c.4966A>T	NP_059989.3:p.Thr1656Ser