Canonical Allele Identifier: CA1675522944
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201083G= , CM000668.2:g.157201083G= GRCh38
NC_000006.11:g.157522217G= , CM000668.1:g.157522217G= GRCh37
NC_000006.10:g.157563909G= NCBI36
NG_032093.1:g.428154G=
NG_032093.2:g.428154G=
NG_066624.1:g.430058G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4699G= ENSP00000055163.8:p.Asp1567=
ENST00000414678.8:c.4768G= ENSP00000412835.3:p.Asp1590=
ENST00000637015.2:c.4987G= ENSP00000489729.2:p.Asp1663=
ENST00000346085.10:c.4738G= ENSP00000344546.5:p.Asp1580=
ENST00000350026.10:c.4450G= ENSP00000055163.7:p.Asp1484=
ENST00000414678.7:c.3016G= ENSP00000412835.2:p.Asp1006=
ENST00000635849.1:c.2179G= ENSP00000490948.1:p.Asp727=
ENST00000635957.1:c.1810G= ENSP00000490385.1:p.Asp604=
ENST00000636227.1:n.3321G=
ENST00000636254.1:n.778G=
ENST00000636930.2:c.4858G= MANE Select ENSP00000490491.2:p.Asp1620=
ENST00000636940.1:n.2855G=
ENST00000637015.1:c.2226G=
ENST00000637568.1:c.2140G=
ENST00000637741.1:n.1524G=
ENST00000637810.1:c.2200G= ENSP00000489636.1:p.Asp734=
ENST00000637904.1:c.2359G= ENSP00000490550.1:p.Asp787=
ENST00000647938.1:c.4489G= ENSP00000498155.1:p.Asp1497=
ENST00000346085.9:c.4489G= ENSP00000344546.4:p.Asp1497=
ENST00000350026.9:c.4450G= ENSP00000055163.7:p.Asp1484=
ENST00000414678.6:c.3016G= ENSP00000412835.2:p.Asp1006=
NM_017519.2:c.4450G= NP_059989.2:p.Asp1484=
NM_020732.3:c.4489G= NP_065783.3:p.Asp1497=
XM_005267069.3:c.4609G= XP_005267126.2:p.Asp1537=
XM_011535984.1:c.3688G= XP_011534286.1:p.Asp1230=
XM_011535985.1:c.3508G= XP_011534287.1:p.Asp1170=
XM_011535986.1:c.3268G= XP_011534288.1:p.Asp1090=
XM_011535987.1:c.2887G= XP_011534289.1:p.Asp963=
XM_011535988.1:c.1750G= XP_011534290.1:p.Asp584=
NM_001346813.1:c.4609G= NP_001333742.1:p.Asp1537=
NM_001363725.1:c.2359G= NP_001350654.1:p.Asp787=
XM_011535984.2:c.4819G= XP_011534286.2:p.Asp1607=
XM_011535988.3:c.1750G= XP_011534290.1:p.Asp584=
XM_017011103.2:c.4720G= XP_016866592.1:p.Asp1574=
XM_017011104.1:c.4690G= XP_016866593.1:p.Asp1564=
XM_017011105.2:c.4660G= XP_016866594.1:p.Asp1554=
XM_017011106.2:c.4531G= XP_016866595.1:p.Asp1511=
XM_017011107.2:c.4510G= XP_016866596.1:p.Asp1504=
XR_002956289.1:n.4805G=
NM_001363725.2:c.2359G= NP_001350654.1:p.Asp787=
NM_001371656.1:c.4738G= NP_001358585.1:p.Asp1580=
NM_001374820.1:c.4738G= NP_001361749.1:p.Asp1580=
NM_001374828.1:c.4858G= MANE Select NP_001361757.1:p.Asp1620=
NM_017519.3:c.4699G= NP_059989.3:p.Asp1567=