Canonical Allele Identifier: CA1675538268
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189757G= , CM000668.2:g.157189757G= GRCh38
NC_000006.11:g.157510891G= , CM000668.1:g.157510891G= GRCh37
NC_000006.10:g.157552583G= NCBI36
NG_032093.1:g.416828G=
NG_032093.2:g.416828G=
NG_066624.1:g.418732G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3876G= ENSP00000055163.8:p.Gln1292=
ENST00000414678.8:c.3945G= ENSP00000412835.3:p.Gln1315=
ENST00000637015.2:c.4164G= ENSP00000489729.2:p.Gln1388=
ENST00000346085.10:c.3915G= ENSP00000344546.5:p.Gln1305=
ENST00000350026.10:c.3627G= ENSP00000055163.7:p.Gln1209=
ENST00000414678.7:c.2193G= ENSP00000412835.2:p.Gln731=
ENST00000635849.1:c.1356G= ENSP00000490948.1:p.Gln452=
ENST00000635957.1:c.990G= ENSP00000490385.1:p.Gln330=
ENST00000636930.2:c.4035G= MANE Select ENSP00000490491.2:p.Gln1345=
ENST00000636940.1:n.2032G=
ENST00000637015.1:c.1403G=
ENST00000637568.1:c.1317G=
ENST00000637741.1:n.701G=
ENST00000637810.1:c.1377G= ENSP00000489636.1:p.Gln459=
ENST00000637904.1:c.1536G= ENSP00000490550.1:p.Gln512=
ENST00000647938.1:c.3666G= ENSP00000498155.1:p.Gln1222=
ENST00000346085.9:c.3666G= ENSP00000344546.4:p.Gln1222=
ENST00000350026.9:c.3627G= ENSP00000055163.7:p.Gln1209=
ENST00000414678.6:c.2193G= ENSP00000412835.2:p.Gln731=
NM_017519.2:c.3627G= NP_059989.2:p.Gln1209=
NM_020732.3:c.3666G= NP_065783.3:p.Gln1222=
XM_005267069.3:c.3786G= XP_005267126.2:p.Gln1262=
XM_011535984.1:c.2865G= XP_011534286.1:p.Gln955=
XM_011535985.1:c.2685G= XP_011534287.1:p.Gln895=
XM_011535986.1:c.2445G= XP_011534288.1:p.Gln815=
XM_011535987.1:c.2064G= XP_011534289.1:p.Gln688=
XM_011535988.1:c.927G= XP_011534290.1:p.Gln309=
NM_001346813.1:c.3786G= NP_001333742.1:p.Gln1262=
NM_001363725.1:c.1536G= NP_001350654.1:p.Gln512=
XM_011535984.2:c.3996G= XP_011534286.2:p.Gln1332=
XM_011535988.3:c.927G= XP_011534290.1:p.Gln309=
XM_017011103.2:c.3897G= XP_016866592.1:p.Gln1299=
XM_017011104.1:c.3867G= XP_016866593.1:p.Gln1289=
XM_017011105.2:c.3837G= XP_016866594.1:p.Gln1279=
XM_017011106.2:c.3708G= XP_016866595.1:p.Gln1236=
XM_017011107.2:c.3687G= XP_016866596.1:p.Gln1229=
XR_002956289.1:n.4079G=
NM_001363725.2:c.1536G= NP_001350654.1:p.Gln512=
NM_001371656.1:c.3915G= NP_001358585.1:p.Gln1305=
NM_001374820.1:c.3915G= NP_001361749.1:p.Gln1305=
NM_001374828.1:c.4035G= MANE Select NP_001361757.1:p.Gln1345=
NM_017519.3:c.3876G= NP_059989.3:p.Gln1292=