Canonical Allele Identifier: CA1675538394
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190074T= , CM000668.2:g.157190074T= GRCh38
NC_000006.11:g.157511208T= , CM000668.1:g.157511208T= GRCh37
NC_000006.10:g.157552900T= NCBI36
NG_032093.1:g.417145T=
NG_032093.2:g.417145T=
NG_066624.1:g.419049T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3936T= ENSP00000055163.8:p.Asp1312=
ENST00000414678.8:c.4005T= ENSP00000412835.3:p.Asp1335=
ENST00000637015.2:c.4224T= ENSP00000489729.2:p.Asp1408=
ENST00000346085.10:c.3975T= ENSP00000344546.5:p.Asp1325=
ENST00000350026.10:c.3687T= ENSP00000055163.7:p.Asp1229=
ENST00000414678.7:c.2253T= ENSP00000412835.2:p.Asp751=
ENST00000635849.1:c.1416T= ENSP00000490948.1:p.Asp472=
ENST00000635957.1:c.1047T= ENSP00000490385.1:p.Asp349=
ENST00000636930.2:c.4095T= MANE Select ENSP00000490491.2:p.Asp1365=
ENST00000636940.1:n.2092T=
ENST00000637015.1:c.1463T=
ENST00000637568.1:c.1377T=
ENST00000637741.1:n.761T=
ENST00000637810.1:c.1437T= ENSP00000489636.1:p.Asp479=
ENST00000637904.1:c.1596T= ENSP00000490550.1:p.Asp532=
ENST00000647938.1:c.3726T= ENSP00000498155.1:p.Asp1242=
ENST00000346085.9:c.3726T= ENSP00000344546.4:p.Asp1242=
ENST00000350026.9:c.3687T= ENSP00000055163.7:p.Asp1229=
ENST00000414678.6:c.2253T= ENSP00000412835.2:p.Asp751=
NM_017519.2:c.3687T= NP_059989.2:p.Asp1229=
NM_020732.3:c.3726T= NP_065783.3:p.Asp1242=
XM_005267069.3:c.3846T= XP_005267126.2:p.Asp1282=
XM_011535984.1:c.2925T= XP_011534286.1:p.Asp975=
XM_011535985.1:c.2745T= XP_011534287.1:p.Asp915=
XM_011535986.1:c.2505T= XP_011534288.1:p.Asp835=
XM_011535987.1:c.2124T= XP_011534289.1:p.Asp708=
XM_011535988.1:c.987T= XP_011534290.1:p.Asp329=
NM_001346813.1:c.3846T= NP_001333742.1:p.Asp1282=
NM_001363725.1:c.1596T= NP_001350654.1:p.Asp532=
XM_011535984.2:c.4056T= XP_011534286.2:p.Asp1352=
XM_011535988.3:c.987T= XP_011534290.1:p.Asp329=
XM_017011103.2:c.3957T= XP_016866592.1:p.Asp1319=
XM_017011104.1:c.3927T= XP_016866593.1:p.Asp1309=
XM_017011105.2:c.3897T= XP_016866594.1:p.Asp1299=
XM_017011106.2:c.3768T= XP_016866595.1:p.Asp1256=
XM_017011107.2:c.3747T= XP_016866596.1:p.Asp1249=
XR_002956289.1:n.4139T=
NM_001363725.2:c.1596T= NP_001350654.1:p.Asp532=
NM_001371656.1:c.3975T= NP_001358585.1:p.Asp1325=
NM_001374820.1:c.3975T= NP_001361749.1:p.Asp1325=
NM_001374828.1:c.4095T= MANE Select NP_001361757.1:p.Asp1365=
NM_017519.3:c.3936T= NP_059989.3:p.Asp1312=