Canonical Allele Identifier: CA1675538233
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189671A= , CM000668.2:g.157189671A= GRCh38
NC_000006.11:g.157510805A= , CM000668.1:g.157510805A= GRCh37
NC_000006.10:g.157552497A= NCBI36
NG_032093.1:g.416742A=
NG_032093.2:g.416742A=
NG_066624.1:g.418646A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3790A= ENSP00000055163.8:p.Thr1264=
ENST00000414678.8:c.3859A= ENSP00000412835.3:p.Thr1287=
ENST00000637015.2:c.4078A= ENSP00000489729.2:p.Thr1360=
ENST00000346085.10:c.3829A= ENSP00000344546.5:p.Thr1277=
ENST00000350026.10:c.3541A= ENSP00000055163.7:p.Thr1181=
ENST00000414678.7:c.2107A= ENSP00000412835.2:p.Thr703=
ENST00000635849.1:c.1270A= ENSP00000490948.1:p.Thr424=
ENST00000635957.1:c.904A= ENSP00000490385.1:p.Thr302=
ENST00000636930.2:c.3949A= MANE Select ENSP00000490491.2:p.Thr1317=
ENST00000636940.1:n.1946A=
ENST00000637015.1:c.1317A=
ENST00000637568.1:c.1231A=
ENST00000637741.1:n.615A=
ENST00000637810.1:c.1291A= ENSP00000489636.1:p.Thr431=
ENST00000637904.1:c.1450A= ENSP00000490550.1:p.Thr484=
ENST00000647938.1:c.3580A= ENSP00000498155.1:p.Thr1194=
ENST00000346085.9:c.3580A= ENSP00000344546.4:p.Thr1194=
ENST00000350026.9:c.3541A= ENSP00000055163.7:p.Thr1181=
ENST00000414678.6:c.2107A= ENSP00000412835.2:p.Thr703=
NM_017519.2:c.3541A= NP_059989.2:p.Thr1181=
NM_020732.3:c.3580A= NP_065783.3:p.Thr1194=
XM_005267069.3:c.3700A= XP_005267126.2:p.Thr1234=
XM_011535984.1:c.2779A= XP_011534286.1:p.Thr927=
XM_011535985.1:c.2599A= XP_011534287.1:p.Thr867=
XM_011535986.1:c.2359A= XP_011534288.1:p.Thr787=
XM_011535987.1:c.1978A= XP_011534289.1:p.Thr660=
XM_011535988.1:c.841A= XP_011534290.1:p.Thr281=
NM_001346813.1:c.3700A= NP_001333742.1:p.Thr1234=
NM_001363725.1:c.1450A= NP_001350654.1:p.Thr484=
XM_011535984.2:c.3910A= XP_011534286.2:p.Thr1304=
XM_011535988.3:c.841A= XP_011534290.1:p.Thr281=
XM_017011103.2:c.3811A= XP_016866592.1:p.Thr1271=
XM_017011104.1:c.3781A= XP_016866593.1:p.Thr1261=
XM_017011105.2:c.3751A= XP_016866594.1:p.Thr1251=
XM_017011106.2:c.3622A= XP_016866595.1:p.Thr1208=
XM_017011107.2:c.3601A= XP_016866596.1:p.Thr1201=
XR_002956289.1:n.3993A=
NM_001363725.2:c.1450A= NP_001350654.1:p.Thr484=
NM_001371656.1:c.3829A= NP_001358585.1:p.Thr1277=
NM_001374820.1:c.3829A= NP_001361749.1:p.Thr1277=
NM_001374828.1:c.3949A= MANE Select NP_001361757.1:p.Thr1317=
NM_017519.3:c.3790A= NP_059989.3:p.Thr1264=