Canonical Allele Identifier: CA1675538234
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189673C= , CM000668.2:g.157189673C= GRCh38
NC_000006.11:g.157510807C= , CM000668.1:g.157510807C= GRCh37
NC_000006.10:g.157552499C= NCBI36
NG_032093.1:g.416744C=
NG_032093.2:g.416744C=
NG_066624.1:g.418648C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3792C= ENSP00000055163.8:p.Thr1264=
ENST00000414678.8:c.3861C= ENSP00000412835.3:p.Thr1287=
ENST00000637015.2:c.4080C= ENSP00000489729.2:p.Thr1360=
ENST00000346085.10:c.3831C= ENSP00000344546.5:p.Thr1277=
ENST00000350026.10:c.3543C= ENSP00000055163.7:p.Thr1181=
ENST00000414678.7:c.2109C= ENSP00000412835.2:p.Thr703=
ENST00000635849.1:c.1272C= ENSP00000490948.1:p.Thr424=
ENST00000635957.1:c.906C= ENSP00000490385.1:p.Thr302=
ENST00000636930.2:c.3951C= MANE Select ENSP00000490491.2:p.Thr1317=
ENST00000636940.1:n.1948C=
ENST00000637015.1:c.1319C=
ENST00000637568.1:c.1233C=
ENST00000637741.1:n.617C=
ENST00000637810.1:c.1293C= ENSP00000489636.1:p.Thr431=
ENST00000637904.1:c.1452C= ENSP00000490550.1:p.Thr484=
ENST00000647938.1:c.3582C= ENSP00000498155.1:p.Thr1194=
ENST00000346085.9:c.3582C= ENSP00000344546.4:p.Thr1194=
ENST00000350026.9:c.3543C= ENSP00000055163.7:p.Thr1181=
ENST00000414678.6:c.2109C= ENSP00000412835.2:p.Thr703=
NM_017519.2:c.3543C= NP_059989.2:p.Thr1181=
NM_020732.3:c.3582C= NP_065783.3:p.Thr1194=
XM_005267069.3:c.3702C= XP_005267126.2:p.Thr1234=
XM_011535984.1:c.2781C= XP_011534286.1:p.Thr927=
XM_011535985.1:c.2601C= XP_011534287.1:p.Thr867=
XM_011535986.1:c.2361C= XP_011534288.1:p.Thr787=
XM_011535987.1:c.1980C= XP_011534289.1:p.Thr660=
XM_011535988.1:c.843C= XP_011534290.1:p.Thr281=
NM_001346813.1:c.3702C= NP_001333742.1:p.Thr1234=
NM_001363725.1:c.1452C= NP_001350654.1:p.Thr484=
XM_011535984.2:c.3912C= XP_011534286.2:p.Thr1304=
XM_011535988.3:c.843C= XP_011534290.1:p.Thr281=
XM_017011103.2:c.3813C= XP_016866592.1:p.Thr1271=
XM_017011104.1:c.3783C= XP_016866593.1:p.Thr1261=
XM_017011105.2:c.3753C= XP_016866594.1:p.Thr1251=
XM_017011106.2:c.3624C= XP_016866595.1:p.Thr1208=
XM_017011107.2:c.3603C= XP_016866596.1:p.Thr1201=
XR_002956289.1:n.3995C=
NM_001363725.2:c.1452C= NP_001350654.1:p.Thr484=
NM_001371656.1:c.3831C= NP_001358585.1:p.Thr1277=
NM_001374820.1:c.3831C= NP_001361749.1:p.Thr1277=
NM_001374828.1:c.3951C= MANE Select NP_001361757.1:p.Thr1317=
NM_017519.3:c.3792C= NP_059989.3:p.Thr1264=