Canonical Allele Identifier: CA366242688

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376135
• gnomAD v4: 6-157201350-A-G
• MyVariant Identifiers: chr6:g.157522484A>G (hg19) ; chr6:g.157201350A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4966A>G	ENSP00000055163.8:p.Thr1656Ala
ENST00000414678.8:c.5035A>G	ENSP00000412835.3:p.Thr1679Ala
ENST00000637015.2:c.5254A>G	ENSP00000489729.2:p.Thr1752Ala
ENST00000346085.10:c.5005A>G	ENSP00000344546.5:p.Thr1669Ala
ENST00000350026.10:c.4717A>G	ENSP00000055163.7:p.Thr1573Ala
ENST00000414678.7:c.3283A>G	ENSP00000412835.2:p.Thr1095Ala
ENST00000635849.1:c.2446A>G	ENSP00000490948.1:p.Thr816Ala
ENST00000635957.1:c.2077A>G	ENSP00000490385.1:p.Thr693Ala
ENST00000636227.1:n.3588A>G
ENST00000636254.1:n.1045A>G
ENST00000636930.2:c.5125A>G MANE Select	ENSP00000490491.2:p.Thr1709Ala
ENST00000636940.1:n.3122A>G
ENST00000637015.1:c.2493A>G
ENST00000637568.1:c.2407A>G
ENST00000637741.1:n.1791A>G
ENST00000637810.1:c.2467A>G	ENSP00000489636.1:p.Thr823Ala
ENST00000637904.1:c.2626A>G	ENSP00000490550.1:p.Thr876Ala
ENST00000647938.1:c.4756A>G	ENSP00000498155.1:p.Thr1586Ala
ENST00000346085.9:c.4756A>G	ENSP00000344546.4:p.Thr1586Ala
ENST00000350026.9:c.4717A>G	ENSP00000055163.7:p.Thr1573Ala
ENST00000414678.6:c.3283A>G	ENSP00000412835.2:p.Thr1095Ala
NM_017519.2:c.4717A>G	NP_059989.2:p.Thr1573Ala
NM_020732.3:c.4756A>G	NP_065783.3:p.Thr1586Ala
XM_005267069.3:c.4876A>G	XP_005267126.2:p.Thr1626Ala
XM_011535984.1:c.3955A>G	XP_011534286.1:p.Thr1319Ala
XM_011535985.1:c.3775A>G	XP_011534287.1:p.Thr1259Ala
XM_011535986.1:c.3535A>G	XP_011534288.1:p.Thr1179Ala
XM_011535987.1:c.3154A>G	XP_011534289.1:p.Thr1052Ala
XM_011535988.1:c.2017A>G	XP_011534290.1:p.Thr673Ala
NM_001346813.1:c.4876A>G	NP_001333742.1:p.Thr1626Ala
NM_001363725.1:c.2626A>G	NP_001350654.1:p.Thr876Ala
XM_011535984.2:c.5086A>G	XP_011534286.2:p.Thr1696Ala
XM_011535988.3:c.2017A>G	XP_011534290.1:p.Thr673Ala
XM_017011103.2:c.4987A>G	XP_016866592.1:p.Thr1663Ala
XM_017011104.1:c.4957A>G	XP_016866593.1:p.Thr1653Ala
XM_017011105.2:c.4927A>G	XP_016866594.1:p.Thr1643Ala
XM_017011106.2:c.4798A>G	XP_016866595.1:p.Thr1600Ala
XM_017011107.2:c.4777A>G	XP_016866596.1:p.Thr1593Ala
XR_002956289.1:n.5072A>G
NM_001363725.2:c.2626A>G	NP_001350654.1:p.Thr876Ala
NM_001371656.1:c.5005A>G	NP_001358585.1:p.Thr1669Ala
NM_001374820.1:c.5005A>G	NP_001361749.1:p.Thr1669Ala
NM_001374828.1:c.5125A>G MANE Select	NP_001361757.1:p.Thr1709Ala
NM_017519.3:c.4966A>G	NP_059989.3:p.Thr1656Ala