Canonical Allele Identifier: CA1675523017
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201123G= , CM000668.2:g.157201123G= GRCh38
NC_000006.11:g.157522257G= , CM000668.1:g.157522257G= GRCh37
NC_000006.10:g.157563949G= NCBI36
NG_032093.1:g.428194G=
NG_032093.2:g.428194G=
NG_066624.1:g.430098G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4739G= ENSP00000055163.8:p.Ser1580=
ENST00000414678.8:c.4808G= ENSP00000412835.3:p.Ser1603=
ENST00000637015.2:c.5027G= ENSP00000489729.2:p.Ser1676=
ENST00000346085.10:c.4778G= ENSP00000344546.5:p.Ser1593=
ENST00000350026.10:c.4490G= ENSP00000055163.7:p.Ser1497=
ENST00000414678.7:c.3056G= ENSP00000412835.2:p.Ser1019=
ENST00000635849.1:c.2219G= ENSP00000490948.1:p.Ser740=
ENST00000635957.1:c.1850G= ENSP00000490385.1:p.Ser617=
ENST00000636227.1:n.3361G=
ENST00000636254.1:n.818G=
ENST00000636930.2:c.4898G= MANE Select ENSP00000490491.2:p.Ser1633=
ENST00000636940.1:n.2895G=
ENST00000637015.1:c.2266G=
ENST00000637568.1:c.2180G=
ENST00000637741.1:n.1564G=
ENST00000637810.1:c.2240G= ENSP00000489636.1:p.Ser747=
ENST00000637904.1:c.2399G= ENSP00000490550.1:p.Ser800=
ENST00000647938.1:c.4529G= ENSP00000498155.1:p.Ser1510=
ENST00000346085.9:c.4529G= ENSP00000344546.4:p.Ser1510=
ENST00000350026.9:c.4490G= ENSP00000055163.7:p.Ser1497=
ENST00000414678.6:c.3056G= ENSP00000412835.2:p.Ser1019=
NM_017519.2:c.4490G= NP_059989.2:p.Ser1497=
NM_020732.3:c.4529G= NP_065783.3:p.Ser1510=
XM_005267069.3:c.4649G= XP_005267126.2:p.Ser1550=
XM_011535984.1:c.3728G= XP_011534286.1:p.Ser1243=
XM_011535985.1:c.3548G= XP_011534287.1:p.Ser1183=
XM_011535986.1:c.3308G= XP_011534288.1:p.Ser1103=
XM_011535987.1:c.2927G= XP_011534289.1:p.Ser976=
XM_011535988.1:c.1790G= XP_011534290.1:p.Ser597=
NM_001346813.1:c.4649G= NP_001333742.1:p.Ser1550=
NM_001363725.1:c.2399G= NP_001350654.1:p.Ser800=
XM_011535984.2:c.4859G= XP_011534286.2:p.Ser1620=
XM_011535988.3:c.1790G= XP_011534290.1:p.Ser597=
XM_017011103.2:c.4760G= XP_016866592.1:p.Ser1587=
XM_017011104.1:c.4730G= XP_016866593.1:p.Ser1577=
XM_017011105.2:c.4700G= XP_016866594.1:p.Ser1567=
XM_017011106.2:c.4571G= XP_016866595.1:p.Ser1524=
XM_017011107.2:c.4550G= XP_016866596.1:p.Ser1517=
XR_002956289.1:n.4845G=
NM_001363725.2:c.2399G= NP_001350654.1:p.Ser800=
NM_001371656.1:c.4778G= NP_001358585.1:p.Ser1593=
NM_001374820.1:c.4778G= NP_001361749.1:p.Ser1593=
NM_001374828.1:c.4898G= MANE Select NP_001361757.1:p.Ser1633=
NM_017519.3:c.4739G= NP_059989.3:p.Ser1580=