Canonical Allele Identifier: CA366242737
Gene: ARID1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201360C>G , CM000668.2:g.157201360C>G GRCh38
NC_000006.11:g.157522494C>G , CM000668.1:g.157522494C>G GRCh37
NC_000006.10:g.157564186C>G NCBI36
NG_032093.1:g.428431C>G
NG_032093.2:g.428431C>G
NG_066624.1:g.430335C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4976C>G ENSP00000055163.8:p.Thr1659Arg
ENST00000414678.8:c.5045C>G ENSP00000412835.3:p.Thr1682Arg
ENST00000637015.2:c.5264C>G ENSP00000489729.2:p.Thr1755Arg
ENST00000346085.10:c.5015C>G ENSP00000344546.5:p.Thr1672Arg
ENST00000350026.10:c.4727C>G ENSP00000055163.7:p.Thr1576Arg
ENST00000414678.7:c.3293C>G ENSP00000412835.2:p.Thr1098Arg
ENST00000635849.1:c.2456C>G ENSP00000490948.1:p.Thr819Arg
ENST00000635957.1:c.2087C>G ENSP00000490385.1:p.Thr696Arg
ENST00000636227.1:n.3598C>G
ENST00000636254.1:n.1055C>G
ENST00000636930.2:c.5135C>G MANE Select ENSP00000490491.2:p.Thr1712Arg
ENST00000636940.1:n.3132C>G
ENST00000637015.1:c.2503C>G
ENST00000637568.1:c.2417C>G
ENST00000637741.1:n.1801C>G
ENST00000637810.1:c.2477C>G ENSP00000489636.1:p.Thr826Arg
ENST00000637904.1:c.2636C>G ENSP00000490550.1:p.Thr879Arg
ENST00000647938.1:c.4766C>G ENSP00000498155.1:p.Thr1589Arg
ENST00000346085.9:c.4766C>G ENSP00000344546.4:p.Thr1589Arg
ENST00000350026.9:c.4727C>G ENSP00000055163.7:p.Thr1576Arg
ENST00000414678.6:c.3293C>G ENSP00000412835.2:p.Thr1098Arg
NM_017519.2:c.4727C>G NP_059989.2:p.Thr1576Arg
NM_020732.3:c.4766C>G NP_065783.3:p.Thr1589Arg
XM_005267069.3:c.4886C>G XP_005267126.2:p.Thr1629Arg
XM_011535984.1:c.3965C>G XP_011534286.1:p.Thr1322Arg
XM_011535985.1:c.3785C>G XP_011534287.1:p.Thr1262Arg
XM_011535986.1:c.3545C>G XP_011534288.1:p.Thr1182Arg
XM_011535987.1:c.3164C>G XP_011534289.1:p.Thr1055Arg
XM_011535988.1:c.2027C>G XP_011534290.1:p.Thr676Arg
NM_001346813.1:c.4886C>G NP_001333742.1:p.Thr1629Arg
NM_001363725.1:c.2636C>G NP_001350654.1:p.Thr879Arg
XM_011535984.2:c.5096C>G XP_011534286.2:p.Thr1699Arg
XM_011535988.3:c.2027C>G XP_011534290.1:p.Thr676Arg
XM_017011103.2:c.4997C>G XP_016866592.1:p.Thr1666Arg
XM_017011104.1:c.4967C>G XP_016866593.1:p.Thr1656Arg
XM_017011105.2:c.4937C>G XP_016866594.1:p.Thr1646Arg
XM_017011106.2:c.4808C>G XP_016866595.1:p.Thr1603Arg
XM_017011107.2:c.4787C>G XP_016866596.1:p.Thr1596Arg
XR_002956289.1:n.5082C>G
NM_001363725.2:c.2636C>G NP_001350654.1:p.Thr879Arg
NM_001371656.1:c.5015C>G NP_001358585.1:p.Thr1672Arg
NM_001374820.1:c.5015C>G NP_001361749.1:p.Thr1672Arg
NM_001374828.1:c.5135C>G MANE Select NP_001361757.1:p.Thr1712Arg
NM_017519.3:c.4976C>G NP_059989.3:p.Thr1659Arg