Canonical Allele Identifier: CA1675523135
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201194C= , CM000668.2:g.157201194C= GRCh38
NC_000006.11:g.157522328C= , CM000668.1:g.157522328C= GRCh37
NC_000006.10:g.157564020C= NCBI36
NG_032093.1:g.428265C=
NG_032093.2:g.428265C=
NG_066624.1:g.430169C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4810C= ENSP00000055163.8:p.Arg1604=
ENST00000414678.8:c.4879C= ENSP00000412835.3:p.Arg1627=
ENST00000637015.2:c.5098C= ENSP00000489729.2:p.Arg1700=
ENST00000346085.10:c.4849C= ENSP00000344546.5:p.Arg1617=
ENST00000350026.10:c.4561C= ENSP00000055163.7:p.Arg1521=
ENST00000414678.7:c.3127C= ENSP00000412835.2:p.Arg1043=
ENST00000635849.1:c.2290C= ENSP00000490948.1:p.Arg764=
ENST00000635957.1:c.1921C= ENSP00000490385.1:p.Arg641=
ENST00000636227.1:n.3432C=
ENST00000636254.1:n.889C=
ENST00000636930.2:c.4969C= MANE Select ENSP00000490491.2:p.Arg1657=
ENST00000636940.1:n.2966C=
ENST00000637015.1:c.2337C=
ENST00000637568.1:c.2251C=
ENST00000637741.1:n.1635C=
ENST00000637810.1:c.2311C= ENSP00000489636.1:p.Arg771=
ENST00000637904.1:c.2470C= ENSP00000490550.1:p.Arg824=
ENST00000647938.1:c.4600C= ENSP00000498155.1:p.Arg1534=
ENST00000346085.9:c.4600C= ENSP00000344546.4:p.Arg1534=
ENST00000350026.9:c.4561C= ENSP00000055163.7:p.Arg1521=
ENST00000414678.6:c.3127C= ENSP00000412835.2:p.Arg1043=
NM_017519.2:c.4561C= NP_059989.2:p.Arg1521=
NM_020732.3:c.4600C= NP_065783.3:p.Arg1534=
XM_005267069.3:c.4720C= XP_005267126.2:p.Arg1574=
XM_011535984.1:c.3799C= XP_011534286.1:p.Arg1267=
XM_011535985.1:c.3619C= XP_011534287.1:p.Arg1207=
XM_011535986.1:c.3379C= XP_011534288.1:p.Arg1127=
XM_011535987.1:c.2998C= XP_011534289.1:p.Arg1000=
XM_011535988.1:c.1861C= XP_011534290.1:p.Arg621=
NM_001346813.1:c.4720C= NP_001333742.1:p.Arg1574=
NM_001363725.1:c.2470C= NP_001350654.1:p.Arg824=
XM_011535984.2:c.4930C= XP_011534286.2:p.Arg1644=
XM_011535988.3:c.1861C= XP_011534290.1:p.Arg621=
XM_017011103.2:c.4831C= XP_016866592.1:p.Arg1611=
XM_017011104.1:c.4801C= XP_016866593.1:p.Arg1601=
XM_017011105.2:c.4771C= XP_016866594.1:p.Arg1591=
XM_017011106.2:c.4642C= XP_016866595.1:p.Arg1548=
XM_017011107.2:c.4621C= XP_016866596.1:p.Arg1541=
XR_002956289.1:n.4916C=
NM_001363725.2:c.2470C= NP_001350654.1:p.Arg824=
NM_001371656.1:c.4849C= NP_001358585.1:p.Arg1617=
NM_001374820.1:c.4849C= NP_001361749.1:p.Arg1617=
NM_001374828.1:c.4969C= MANE Select NP_001361757.1:p.Arg1657=
NM_017519.3:c.4810C= NP_059989.3:p.Arg1604=