Canonical Allele Identifier: CA1675523048
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201142C= , CM000668.2:g.157201142C= GRCh38
NC_000006.11:g.157522276C= , CM000668.1:g.157522276C= GRCh37
NC_000006.10:g.157563968C= NCBI36
NG_032093.1:g.428213C=
NG_032093.2:g.428213C=
NG_066624.1:g.430117C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4758C= ENSP00000055163.8:p.Val1586=
ENST00000414678.8:c.4827C= ENSP00000412835.3:p.Val1609=
ENST00000637015.2:c.5046C= ENSP00000489729.2:p.Val1682=
ENST00000346085.10:c.4797C= ENSP00000344546.5:p.Val1599=
ENST00000350026.10:c.4509C= ENSP00000055163.7:p.Val1503=
ENST00000414678.7:c.3075C= ENSP00000412835.2:p.Val1025=
ENST00000635849.1:c.2238C= ENSP00000490948.1:p.Val746=
ENST00000635957.1:c.1869C= ENSP00000490385.1:p.Val623=
ENST00000636227.1:n.3380C=
ENST00000636254.1:n.837C=
ENST00000636930.2:c.4917C= MANE Select ENSP00000490491.2:p.Val1639=
ENST00000636940.1:n.2914C=
ENST00000637015.1:c.2285C=
ENST00000637568.1:c.2199C=
ENST00000637741.1:n.1583C=
ENST00000637810.1:c.2259C= ENSP00000489636.1:p.Val753=
ENST00000637904.1:c.2418C= ENSP00000490550.1:p.Val806=
ENST00000647938.1:c.4548C= ENSP00000498155.1:p.Val1516=
ENST00000346085.9:c.4548C= ENSP00000344546.4:p.Val1516=
ENST00000350026.9:c.4509C= ENSP00000055163.7:p.Val1503=
ENST00000414678.6:c.3075C= ENSP00000412835.2:p.Val1025=
NM_017519.2:c.4509C= NP_059989.2:p.Val1503=
NM_020732.3:c.4548C= NP_065783.3:p.Val1516=
XM_005267069.3:c.4668C= XP_005267126.2:p.Val1556=
XM_011535984.1:c.3747C= XP_011534286.1:p.Val1249=
XM_011535985.1:c.3567C= XP_011534287.1:p.Val1189=
XM_011535986.1:c.3327C= XP_011534288.1:p.Val1109=
XM_011535987.1:c.2946C= XP_011534289.1:p.Val982=
XM_011535988.1:c.1809C= XP_011534290.1:p.Val603=
NM_001346813.1:c.4668C= NP_001333742.1:p.Val1556=
NM_001363725.1:c.2418C= NP_001350654.1:p.Val806=
XM_011535984.2:c.4878C= XP_011534286.2:p.Val1626=
XM_011535988.3:c.1809C= XP_011534290.1:p.Val603=
XM_017011103.2:c.4779C= XP_016866592.1:p.Val1593=
XM_017011104.1:c.4749C= XP_016866593.1:p.Val1583=
XM_017011105.2:c.4719C= XP_016866594.1:p.Val1573=
XM_017011106.2:c.4590C= XP_016866595.1:p.Val1530=
XM_017011107.2:c.4569C= XP_016866596.1:p.Val1523=
XR_002956289.1:n.4864C=
NM_001363725.2:c.2418C= NP_001350654.1:p.Val806=
NM_001371656.1:c.4797C= NP_001358585.1:p.Val1599=
NM_001374820.1:c.4797C= NP_001361749.1:p.Val1599=
NM_001374828.1:c.4917C= MANE Select NP_001361757.1:p.Val1639=
NM_017519.3:c.4758C= NP_059989.3:p.Val1586=