Canonical Allele Identifier: CA1675538225
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189654C= , CM000668.2:g.157189654C= GRCh38
NC_000006.11:g.157510788C= , CM000668.1:g.157510788C= GRCh37
NC_000006.10:g.157552480C= NCBI36
NG_032093.1:g.416725C=
NG_032093.2:g.416725C=
NG_066624.1:g.418629C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3773C= ENSP00000055163.8:p.Ser1258=
ENST00000414678.8:c.3842C= ENSP00000412835.3:p.Ser1281=
ENST00000637015.2:c.4061C= ENSP00000489729.2:p.Ser1354=
ENST00000346085.10:c.3812C= ENSP00000344546.5:p.Ser1271=
ENST00000350026.10:c.3524C= ENSP00000055163.7:p.Ser1175=
ENST00000414678.7:c.2090C= ENSP00000412835.2:p.Ser697=
ENST00000635849.1:c.1253C= ENSP00000490948.1:p.Ser418=
ENST00000635957.1:c.887C= ENSP00000490385.1:p.Ser296=
ENST00000636930.2:c.3932C= MANE Select ENSP00000490491.2:p.Ser1311=
ENST00000636940.1:n.1929C=
ENST00000637015.1:c.1300C=
ENST00000637568.1:c.1214C=
ENST00000637741.1:n.598C=
ENST00000637810.1:c.1274C= ENSP00000489636.1:p.Ser425=
ENST00000637904.1:c.1433C= ENSP00000490550.1:p.Ser478=
ENST00000647938.1:c.3563C= ENSP00000498155.1:p.Ser1188=
ENST00000346085.9:c.3563C= ENSP00000344546.4:p.Ser1188=
ENST00000350026.9:c.3524C= ENSP00000055163.7:p.Ser1175=
ENST00000414678.6:c.2090C= ENSP00000412835.2:p.Ser697=
NM_017519.2:c.3524C= NP_059989.2:p.Ser1175=
NM_020732.3:c.3563C= NP_065783.3:p.Ser1188=
XM_005267069.3:c.3683C= XP_005267126.2:p.Ser1228=
XM_011535984.1:c.2762C= XP_011534286.1:p.Ser921=
XM_011535985.1:c.2582C= XP_011534287.1:p.Ser861=
XM_011535986.1:c.2342C= XP_011534288.1:p.Ser781=
XM_011535987.1:c.1961C= XP_011534289.1:p.Ser654=
XM_011535988.1:c.824C= XP_011534290.1:p.Ser275=
NM_001346813.1:c.3683C= NP_001333742.1:p.Ser1228=
NM_001363725.1:c.1433C= NP_001350654.1:p.Ser478=
XM_011535984.2:c.3893C= XP_011534286.2:p.Ser1298=
XM_011535988.3:c.824C= XP_011534290.1:p.Ser275=
XM_017011103.2:c.3794C= XP_016866592.1:p.Ser1265=
XM_017011104.1:c.3764C= XP_016866593.1:p.Ser1255=
XM_017011105.2:c.3734C= XP_016866594.1:p.Ser1245=
XM_017011106.2:c.3605C= XP_016866595.1:p.Ser1202=
XM_017011107.2:c.3584C= XP_016866596.1:p.Ser1195=
XR_002956289.1:n.3976C=
NM_001363725.2:c.1433C= NP_001350654.1:p.Ser478=
NM_001371656.1:c.3812C= NP_001358585.1:p.Ser1271=
NM_001374820.1:c.3812C= NP_001361749.1:p.Ser1271=
NM_001374828.1:c.3932C= MANE Select NP_001361757.1:p.Ser1311=
NM_017519.3:c.3773C= NP_059989.3:p.Ser1258=