Canonical Allele Identifier: CA4067630
Gene: ARID1B HGNC NCBI

Linked Data

dbSNP Id: rs765570329

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157198903A>G , CM000668.2:g.157198903A>G GRCh38
NC_000006.11:g.157520037A>G , CM000668.1:g.157520037A>G GRCh37
NC_000006.10:g.157561729A>G NCBI36
NG_032093.1:g.425974A>G
NG_032093.2:g.425974A>G
NG_066624.1:g.427878A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4316A>G ENSP00000055163.8:p.Gln1439Arg
ENST00000414678.8:c.4385A>G ENSP00000412835.3:p.Gln1462Arg
ENST00000637015.2:c.4604A>G ENSP00000489729.2:p.Gln1535Arg
ENST00000346085.10:c.4355A>G ENSP00000344546.5:p.Gln1452Arg
ENST00000350026.10:c.4067A>G ENSP00000055163.7:p.Gln1356Arg
ENST00000414678.7:c.2633A>G ENSP00000412835.2:p.Gln878Arg
ENST00000635849.1:c.1796A>G ENSP00000490948.1:p.Gln599Arg
ENST00000635957.1:c.1427A>G ENSP00000490385.1:p.Gln476Arg
ENST00000636227.1:n.2938A>G
ENST00000636254.1:n.395A>G
ENST00000636930.2:c.4475A>G MANE Select ENSP00000490491.2:p.Gln1492Arg
ENST00000636940.1:n.2472A>G
ENST00000637015.1:c.1843A>G
ENST00000637568.1:c.1757A>G
ENST00000637741.1:n.1141A>G
ENST00000637810.1:c.1817A>G ENSP00000489636.1:p.Gln606Arg
ENST00000637904.1:c.1976A>G ENSP00000490550.1:p.Gln659Arg
ENST00000647938.1:c.4106A>G ENSP00000498155.1:p.Gln1369Arg
ENST00000346085.9:c.4106A>G ENSP00000344546.4:p.Gln1369Arg
ENST00000350026.9:c.4067A>G ENSP00000055163.7:p.Gln1356Arg
ENST00000414678.6:c.2633A>G ENSP00000412835.2:p.Gln878Arg
NM_017519.2:c.4067A>G NP_059989.2:p.Gln1356Arg
NM_020732.3:c.4106A>G NP_065783.3:p.Gln1369Arg
XM_005267069.3:c.4226A>G XP_005267126.2:p.Gln1409Arg
XM_011535984.1:c.3305A>G XP_011534286.1:p.Gln1102Arg
XM_011535985.1:c.3125A>G XP_011534287.1:p.Gln1042Arg
XM_011535986.1:c.2885A>G XP_011534288.1:p.Gln962Arg
XM_011535987.1:c.2504A>G XP_011534289.1:p.Gln835Arg
XM_011535988.1:c.1367A>G XP_011534290.1:p.Gln456Arg
NM_001346813.1:c.4226A>G NP_001333742.1:p.Gln1409Arg
NM_001363725.1:c.1976A>G NP_001350654.1:p.Gln659Arg
XM_011535984.2:c.4436A>G XP_011534286.2:p.Gln1479Arg
XM_011535988.3:c.1367A>G XP_011534290.1:p.Gln456Arg
XM_017011103.2:c.4337A>G XP_016866592.1:p.Gln1446Arg
XM_017011104.1:c.4307A>G XP_016866593.1:p.Gln1436Arg
XM_017011105.2:c.4277A>G XP_016866594.1:p.Gln1426Arg
XM_017011106.2:c.4148A>G XP_016866595.1:p.Gln1383Arg
XM_017011107.2:c.4127A>G XP_016866596.1:p.Gln1376Arg
XR_002956289.1:n.4427-1802A>G
NM_001363725.2:c.1976A>G NP_001350654.1:p.Gln659Arg
NM_001371656.1:c.4355A>G NP_001358585.1:p.Gln1452Arg
NM_001374820.1:c.4355A>G NP_001361749.1:p.Gln1452Arg
NM_001374828.1:c.4475A>G MANE Select NP_001361757.1:p.Gln1492Arg
NM_017519.3:c.4316A>G NP_059989.3:p.Gln1439Arg