Canonical Allele Identifier: CA1675538385
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190051A= , CM000668.2:g.157190051A= GRCh38
NC_000006.11:g.157511185A= , CM000668.1:g.157511185A= GRCh37
NC_000006.10:g.157552877A= NCBI36
NG_032093.1:g.417122A=
NG_032093.2:g.417122A=
NG_066624.1:g.419026A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3913A= ENSP00000055163.8:p.Ser1305=
ENST00000414678.8:c.3982A= ENSP00000412835.3:p.Ser1328=
ENST00000637015.2:c.4201A= ENSP00000489729.2:p.Ser1401=
ENST00000346085.10:c.3952A= ENSP00000344546.5:p.Ser1318=
ENST00000350026.10:c.3664A= ENSP00000055163.7:p.Ser1222=
ENST00000414678.7:c.2230A= ENSP00000412835.2:p.Ser744=
ENST00000635849.1:c.1393A= ENSP00000490948.1:p.Ser465=
ENST00000635957.1:c.1024A= ENSP00000490385.1:p.Ser342=
ENST00000636930.2:c.4072A= MANE Select ENSP00000490491.2:p.Ser1358=
ENST00000636940.1:n.2069A=
ENST00000637015.1:c.1440A=
ENST00000637568.1:c.1354A=
ENST00000637741.1:n.738A=
ENST00000637810.1:c.1414A= ENSP00000489636.1:p.Ser472=
ENST00000637904.1:c.1573A= ENSP00000490550.1:p.Ser525=
ENST00000647938.1:c.3703A= ENSP00000498155.1:p.Ser1235=
ENST00000346085.9:c.3703A= ENSP00000344546.4:p.Ser1235=
ENST00000350026.9:c.3664A= ENSP00000055163.7:p.Ser1222=
ENST00000414678.6:c.2230A= ENSP00000412835.2:p.Ser744=
NM_017519.2:c.3664A= NP_059989.2:p.Ser1222=
NM_020732.3:c.3703A= NP_065783.3:p.Ser1235=
XM_005267069.3:c.3823A= XP_005267126.2:p.Ser1275=
XM_011535984.1:c.2902A= XP_011534286.1:p.Ser968=
XM_011535985.1:c.2722A= XP_011534287.1:p.Ser908=
XM_011535986.1:c.2482A= XP_011534288.1:p.Ser828=
XM_011535987.1:c.2101A= XP_011534289.1:p.Ser701=
XM_011535988.1:c.964A= XP_011534290.1:p.Ser322=
NM_001346813.1:c.3823A= NP_001333742.1:p.Ser1275=
NM_001363725.1:c.1573A= NP_001350654.1:p.Ser525=
XM_011535984.2:c.4033A= XP_011534286.2:p.Ser1345=
XM_011535988.3:c.964A= XP_011534290.1:p.Ser322=
XM_017011103.2:c.3934A= XP_016866592.1:p.Ser1312=
XM_017011104.1:c.3904A= XP_016866593.1:p.Ser1302=
XM_017011105.2:c.3874A= XP_016866594.1:p.Ser1292=
XM_017011106.2:c.3745A= XP_016866595.1:p.Ser1249=
XM_017011107.2:c.3724A= XP_016866596.1:p.Ser1242=
XR_002956289.1:n.4116A=
NM_001363725.2:c.1573A= NP_001350654.1:p.Ser525=
NM_001371656.1:c.3952A= NP_001358585.1:p.Ser1318=
NM_001374820.1:c.3952A= NP_001361749.1:p.Ser1318=
NM_001374828.1:c.4072A= MANE Select NP_001361757.1:p.Ser1358=
NM_017519.3:c.3913A= NP_059989.3:p.Ser1305=