Canonical Allele Identifier: CA2695207232
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157084819dup , CM000668.2:g.157084819dup GRCh38
NC_000006.11:g.157405953dup , CM000668.1:g.157405953dup GRCh37
NC_000006.10:g.157447645dup NCBI36
NG_032093.1:g.311890dup
NG_032093.2:g.311890dup
NG_066624.1:g.313794dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.2405dup ENSP00000055163.8:p.Ser806IlefsTer27
ENST00000414678.8:c.2405dup ENSP00000412835.3:p.Ser806IlefsTer?
ENST00000637015.2:c.2405dup ENSP00000489729.2:p.Ser806IlefsTer27
ENST00000319584.11:c.419dup ENSP00000313006.7:p.Ser144IlefsTer27
ENST00000346085.10:c.2444dup ENSP00000344546.5:p.Ser819IlefsTer27
ENST00000350026.10:c.2156dup ENSP00000055163.7:p.Ser723IlefsTer27
ENST00000414678.7:c.653dup ENSP00000412835.2:p.Ser222IlefsTer?
ENST00000452544.2:n.306dup
ENST00000493658.2:n.54dup
ENST00000635849.1:c.-95dup ENSP00000490948.1:n.-95dup
ENST00000636930.2:c.2405dup MANE Select ENSP00000490491.2:p.Ser806IlefsTer27
ENST00000637003.1:c.-95dup ENSP00000489666.1:n.-95dup
ENST00000637810.1:c.-95dup ENSP00000489636.1:n.-95dup
ENST00000637904.1:c.-95dup ENSP00000490550.1:n.-95dup
ENST00000647938.1:c.2195dup ENSP00000498155.1:p.Ser736IlefsTer27
ENST00000674190.1:n.1154dup
ENST00000319584.10:c.422dup ENSP00000313006.6:p.Ser145IlefsTer27
ENST00000346085.9:c.2195dup ENSP00000344546.4:p.Ser736IlefsTer27
ENST00000350026.9:c.2156dup ENSP00000055163.7:p.Ser723IlefsTer27
ENST00000414678.6:c.653dup ENSP00000412835.2:p.Ser222IlefsTer?
ENST00000452544.1:n.264dup
ENST00000493658.1:n.54dup
NM_017519.2:c.2156dup NP_059989.2:p.Ser723IlefsTer27
NM_020732.3:c.2195dup NP_065783.3:p.Ser736IlefsTer27
XM_005267069.3:c.2156dup XP_005267126.2:p.Ser723IlefsTer27
XM_011535984.1:c.1106dup XP_011534286.1:p.Ser373IlefsTer27
XM_011535985.1:c.1106dup XP_011534287.1:p.Ser373IlefsTer27
XM_011535986.1:c.686dup XP_011534288.1:p.Ser233IlefsTer27
XM_011535987.1:c.305dup XP_011534289.1:p.Ser106IlefsTer27
NM_001346813.1:c.2156dup NP_001333742.1:p.Ser723IlefsTer27
NM_001363725.1:c.-95dup NP_001350654.1:n.-95dup
XM_011535984.2:c.2237dup XP_011534286.2:p.Ser750IlefsTer27
XM_017011103.2:c.2237dup XP_016866592.1:p.Ser750IlefsTer27
XM_017011104.1:c.2237dup XP_016866593.1:p.Ser750IlefsTer27
XM_017011105.2:c.2237dup XP_016866594.1:p.Ser750IlefsTer27
XM_017011106.2:c.2237dup XP_016866595.1:p.Ser750IlefsTer27
XM_017011107.2:c.2237dup XP_016866596.1:p.Ser750IlefsTer27
XR_002956289.1:n.2320dup
NM_001363725.2:c.-95dup NP_001350654.1:n.-95dup
NM_001371656.1:c.2444dup NP_001358585.1:p.Ser819IlefsTer27
NM_001374820.1:c.2444dup NP_001361749.1:p.Ser819IlefsTer27
NM_001374828.1:c.2405dup MANE Select NP_001361757.1:p.Ser806IlefsTer27
NM_017519.3:c.2405dup NP_059989.3:p.Ser806IlefsTer27