Canonical Allele Identifier: CA1675538251
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189717A= , CM000668.2:g.157189717A= GRCh38
NC_000006.11:g.157510851A= , CM000668.1:g.157510851A= GRCh37
NC_000006.10:g.157552543A= NCBI36
NG_032093.1:g.416788A=
NG_032093.2:g.416788A=
NG_066624.1:g.418692A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3836A= ENSP00000055163.8:p.Asp1279=
ENST00000414678.8:c.3905A= ENSP00000412835.3:p.Asp1302=
ENST00000637015.2:c.4124A= ENSP00000489729.2:p.Asp1375=
ENST00000346085.10:c.3875A= ENSP00000344546.5:p.Asp1292=
ENST00000350026.10:c.3587A= ENSP00000055163.7:p.Asp1196=
ENST00000414678.7:c.2153A= ENSP00000412835.2:p.Asp718=
ENST00000635849.1:c.1316A= ENSP00000490948.1:p.Asp439=
ENST00000635957.1:c.950A= ENSP00000490385.1:p.Asp317=
ENST00000636930.2:c.3995A= MANE Select ENSP00000490491.2:p.Asp1332=
ENST00000636940.1:n.1992A=
ENST00000637015.1:c.1363A=
ENST00000637568.1:c.1277A=
ENST00000637741.1:n.661A=
ENST00000637810.1:c.1337A= ENSP00000489636.1:p.Asp446=
ENST00000637904.1:c.1496A= ENSP00000490550.1:p.Asp499=
ENST00000647938.1:c.3626A= ENSP00000498155.1:p.Asp1209=
ENST00000346085.9:c.3626A= ENSP00000344546.4:p.Asp1209=
ENST00000350026.9:c.3587A= ENSP00000055163.7:p.Asp1196=
ENST00000414678.6:c.2153A= ENSP00000412835.2:p.Asp718=
NM_017519.2:c.3587A= NP_059989.2:p.Asp1196=
NM_020732.3:c.3626A= NP_065783.3:p.Asp1209=
XM_005267069.3:c.3746A= XP_005267126.2:p.Asp1249=
XM_011535984.1:c.2825A= XP_011534286.1:p.Asp942=
XM_011535985.1:c.2645A= XP_011534287.1:p.Asp882=
XM_011535986.1:c.2405A= XP_011534288.1:p.Asp802=
XM_011535987.1:c.2024A= XP_011534289.1:p.Asp675=
XM_011535988.1:c.887A= XP_011534290.1:p.Asp296=
NM_001346813.1:c.3746A= NP_001333742.1:p.Asp1249=
NM_001363725.1:c.1496A= NP_001350654.1:p.Asp499=
XM_011535984.2:c.3956A= XP_011534286.2:p.Asp1319=
XM_011535988.3:c.887A= XP_011534290.1:p.Asp296=
XM_017011103.2:c.3857A= XP_016866592.1:p.Asp1286=
XM_017011104.1:c.3827A= XP_016866593.1:p.Asp1276=
XM_017011105.2:c.3797A= XP_016866594.1:p.Asp1266=
XM_017011106.2:c.3668A= XP_016866595.1:p.Asp1223=
XM_017011107.2:c.3647A= XP_016866596.1:p.Asp1216=
XR_002956289.1:n.4039A=
NM_001363725.2:c.1496A= NP_001350654.1:p.Asp499=
NM_001371656.1:c.3875A= NP_001358585.1:p.Asp1292=
NM_001374820.1:c.3875A= NP_001361749.1:p.Asp1292=
NM_001374828.1:c.3995A= MANE Select NP_001361757.1:p.Asp1332=
NM_017519.3:c.3836A= NP_059989.3:p.Asp1279=