Canonical Allele Identifier: CA1675522994
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201111T= , CM000668.2:g.157201111T= GRCh38
NC_000006.11:g.157522245T= , CM000668.1:g.157522245T= GRCh37
NC_000006.10:g.157563937T= NCBI36
NG_032093.1:g.428182T=
NG_032093.2:g.428182T=
NG_066624.1:g.430086T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4727T= ENSP00000055163.8:p.Ile1576=
ENST00000414678.8:c.4796T= ENSP00000412835.3:p.Ile1599=
ENST00000637015.2:c.5015T= ENSP00000489729.2:p.Ile1672=
ENST00000346085.10:c.4766T= ENSP00000344546.5:p.Ile1589=
ENST00000350026.10:c.4478T= ENSP00000055163.7:p.Ile1493=
ENST00000414678.7:c.3044T= ENSP00000412835.2:p.Ile1015=
ENST00000635849.1:c.2207T= ENSP00000490948.1:p.Ile736=
ENST00000635957.1:c.1838T= ENSP00000490385.1:p.Ile613=
ENST00000636227.1:n.3349T=
ENST00000636254.1:n.806T=
ENST00000636930.2:c.4886T= MANE Select ENSP00000490491.2:p.Ile1629=
ENST00000636940.1:n.2883T=
ENST00000637015.1:c.2254T=
ENST00000637568.1:c.2168T=
ENST00000637741.1:n.1552T=
ENST00000637810.1:c.2228T= ENSP00000489636.1:p.Ile743=
ENST00000637904.1:c.2387T= ENSP00000490550.1:p.Ile796=
ENST00000647938.1:c.4517T= ENSP00000498155.1:p.Ile1506=
ENST00000346085.9:c.4517T= ENSP00000344546.4:p.Ile1506=
ENST00000350026.9:c.4478T= ENSP00000055163.7:p.Ile1493=
ENST00000414678.6:c.3044T= ENSP00000412835.2:p.Ile1015=
NM_017519.2:c.4478T= NP_059989.2:p.Ile1493=
NM_020732.3:c.4517T= NP_065783.3:p.Ile1506=
XM_005267069.3:c.4637T= XP_005267126.2:p.Ile1546=
XM_011535984.1:c.3716T= XP_011534286.1:p.Ile1239=
XM_011535985.1:c.3536T= XP_011534287.1:p.Ile1179=
XM_011535986.1:c.3296T= XP_011534288.1:p.Ile1099=
XM_011535987.1:c.2915T= XP_011534289.1:p.Ile972=
XM_011535988.1:c.1778T= XP_011534290.1:p.Ile593=
NM_001346813.1:c.4637T= NP_001333742.1:p.Ile1546=
NM_001363725.1:c.2387T= NP_001350654.1:p.Ile796=
XM_011535984.2:c.4847T= XP_011534286.2:p.Ile1616=
XM_011535988.3:c.1778T= XP_011534290.1:p.Ile593=
XM_017011103.2:c.4748T= XP_016866592.1:p.Ile1583=
XM_017011104.1:c.4718T= XP_016866593.1:p.Ile1573=
XM_017011105.2:c.4688T= XP_016866594.1:p.Ile1563=
XM_017011106.2:c.4559T= XP_016866595.1:p.Ile1520=
XM_017011107.2:c.4538T= XP_016866596.1:p.Ile1513=
XR_002956289.1:n.4833T=
NM_001363725.2:c.2387T= NP_001350654.1:p.Ile796=
NM_001371656.1:c.4766T= NP_001358585.1:p.Ile1589=
NM_001374820.1:c.4766T= NP_001361749.1:p.Ile1589=
NM_001374828.1:c.4886T= MANE Select NP_001361757.1:p.Ile1629=
NM_017519.3:c.4727T= NP_059989.3:p.Ile1576=