Canonical Allele Identifier: CA1675522807
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201003A= , CM000668.2:g.157201003A= GRCh38
NC_000006.11:g.157522137A= , CM000668.1:g.157522137A= GRCh37
NC_000006.10:g.157563829A= NCBI36
NG_032093.1:g.428074A=
NG_032093.2:g.428074A=
NG_066624.1:g.429978A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4619A= ENSP00000055163.8:p.Asp1540=
ENST00000414678.8:c.4688A= ENSP00000412835.3:p.Asp1563=
ENST00000637015.2:c.4907A= ENSP00000489729.2:p.Asp1636=
ENST00000346085.10:c.4658A= ENSP00000344546.5:p.Asp1553=
ENST00000350026.10:c.4370A= ENSP00000055163.7:p.Asp1457=
ENST00000414678.7:c.2936A= ENSP00000412835.2:p.Asp979=
ENST00000635849.1:c.2099A= ENSP00000490948.1:p.Asp700=
ENST00000635957.1:c.1730A= ENSP00000490385.1:p.Asp577=
ENST00000636227.1:n.3241A=
ENST00000636254.1:n.698A=
ENST00000636930.2:c.4778A= MANE Select ENSP00000490491.2:p.Asp1593=
ENST00000636940.1:n.2775A=
ENST00000637015.1:c.2146A=
ENST00000637568.1:c.2060A=
ENST00000637741.1:n.1444A=
ENST00000637810.1:c.2120A= ENSP00000489636.1:p.Asp707=
ENST00000637904.1:c.2279A= ENSP00000490550.1:p.Asp760=
ENST00000647938.1:c.4409A= ENSP00000498155.1:p.Asp1470=
ENST00000346085.9:c.4409A= ENSP00000344546.4:p.Asp1470=
ENST00000350026.9:c.4370A= ENSP00000055163.7:p.Asp1457=
ENST00000414678.6:c.2936A= ENSP00000412835.2:p.Asp979=
NM_017519.2:c.4370A= NP_059989.2:p.Asp1457=
NM_020732.3:c.4409A= NP_065783.3:p.Asp1470=
XM_005267069.3:c.4529A= XP_005267126.2:p.Asp1510=
XM_011535984.1:c.3608A= XP_011534286.1:p.Asp1203=
XM_011535985.1:c.3428A= XP_011534287.1:p.Asp1143=
XM_011535986.1:c.3188A= XP_011534288.1:p.Asp1063=
XM_011535987.1:c.2807A= XP_011534289.1:p.Asp936=
XM_011535988.1:c.1670A= XP_011534290.1:p.Asp557=
NM_001346813.1:c.4529A= NP_001333742.1:p.Asp1510=
NM_001363725.1:c.2279A= NP_001350654.1:p.Asp760=
XM_011535984.2:c.4739A= XP_011534286.2:p.Asp1580=
XM_011535988.3:c.1670A= XP_011534290.1:p.Asp557=
XM_017011103.2:c.4640A= XP_016866592.1:p.Asp1547=
XM_017011104.1:c.4610A= XP_016866593.1:p.Asp1537=
XM_017011105.2:c.4580A= XP_016866594.1:p.Asp1527=
XM_017011106.2:c.4451A= XP_016866595.1:p.Asp1484=
XM_017011107.2:c.4430A= XP_016866596.1:p.Asp1477=
XR_002956289.1:n.4725A=
NM_001363725.2:c.2279A= NP_001350654.1:p.Asp760=
NM_001371656.1:c.4658A= NP_001358585.1:p.Asp1553=
NM_001374820.1:c.4658A= NP_001361749.1:p.Asp1553=
NM_001374828.1:c.4778A= MANE Select NP_001361757.1:p.Asp1593=
NM_017519.3:c.4619A= NP_059989.3:p.Asp1540=