Canonical Allele Identifier: CA1675523513
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201375G= , CM000668.2:g.157201375G= GRCh38
NC_000006.11:g.157522509G= , CM000668.1:g.157522509G= GRCh37
NC_000006.10:g.157564201G= NCBI36
NG_032093.1:g.428446G=
NG_032093.2:g.428446G=
NG_066624.1:g.430350G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4991G= ENSP00000055163.8:p.Gly1664=
ENST00000414678.8:c.5060G= ENSP00000412835.3:p.Gly1687=
ENST00000637015.2:c.5279G= ENSP00000489729.2:p.Gly1760=
ENST00000346085.10:c.5030G= ENSP00000344546.5:p.Gly1677=
ENST00000350026.10:c.4742G= ENSP00000055163.7:p.Gly1581=
ENST00000414678.7:c.3308G= ENSP00000412835.2:p.Gly1103=
ENST00000635849.1:c.2471G= ENSP00000490948.1:p.Gly824=
ENST00000635957.1:c.2102G= ENSP00000490385.1:p.Gly701=
ENST00000636227.1:n.3613G=
ENST00000636254.1:n.1070G=
ENST00000636930.2:c.5150G= MANE Select ENSP00000490491.2:p.Gly1717=
ENST00000636940.1:n.3147G=
ENST00000637015.1:c.2518G=
ENST00000637568.1:c.2432G=
ENST00000637741.1:n.1816G=
ENST00000637810.1:c.2492G= ENSP00000489636.1:p.Gly831=
ENST00000637904.1:c.2651G= ENSP00000490550.1:p.Gly884=
ENST00000647938.1:c.4781G= ENSP00000498155.1:p.Gly1594=
ENST00000346085.9:c.4781G= ENSP00000344546.4:p.Gly1594=
ENST00000350026.9:c.4742G= ENSP00000055163.7:p.Gly1581=
ENST00000414678.6:c.3308G= ENSP00000412835.2:p.Gly1103=
NM_017519.2:c.4742G= NP_059989.2:p.Gly1581=
NM_020732.3:c.4781G= NP_065783.3:p.Gly1594=
XM_005267069.3:c.4901G= XP_005267126.2:p.Gly1634=
XM_011535984.1:c.3980G= XP_011534286.1:p.Gly1327=
XM_011535985.1:c.3800G= XP_011534287.1:p.Gly1267=
XM_011535986.1:c.3560G= XP_011534288.1:p.Gly1187=
XM_011535987.1:c.3179G= XP_011534289.1:p.Gly1060=
XM_011535988.1:c.2042G= XP_011534290.1:p.Gly681=
NM_001346813.1:c.4901G= NP_001333742.1:p.Gly1634=
NM_001363725.1:c.2651G= NP_001350654.1:p.Gly884=
XM_011535984.2:c.5111G= XP_011534286.2:p.Gly1704=
XM_011535988.3:c.2042G= XP_011534290.1:p.Gly681=
XM_017011103.2:c.5012G= XP_016866592.1:p.Gly1671=
XM_017011104.1:c.4982G= XP_016866593.1:p.Gly1661=
XM_017011105.2:c.4952G= XP_016866594.1:p.Gly1651=
XM_017011106.2:c.4823G= XP_016866595.1:p.Gly1608=
XM_017011107.2:c.4802G= XP_016866596.1:p.Gly1601=
XR_002956289.1:n.5097G=
NM_001363725.2:c.2651G= NP_001350654.1:p.Gly884=
NM_001371656.1:c.5030G= NP_001358585.1:p.Gly1677=
NM_001374820.1:c.5030G= NP_001361749.1:p.Gly1677=
NM_001374828.1:c.5150G= MANE Select NP_001361757.1:p.Gly1717=
NM_017519.3:c.4991G= NP_059989.3:p.Gly1664=