Canonical Allele Identifier: CA1675523053
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201146C= , CM000668.2:g.157201146C= GRCh38
NC_000006.11:g.157522280C= , CM000668.1:g.157522280C= GRCh37
NC_000006.10:g.157563972C= NCBI36
NG_032093.1:g.428217C=
NG_032093.2:g.428217C=
NG_066624.1:g.430121C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4762C= ENSP00000055163.8:p.Gln1588=
ENST00000414678.8:c.4831C= ENSP00000412835.3:p.Gln1611=
ENST00000637015.2:c.5050C= ENSP00000489729.2:p.Gln1684=
ENST00000346085.10:c.4801C= ENSP00000344546.5:p.Gln1601=
ENST00000350026.10:c.4513C= ENSP00000055163.7:p.Gln1505=
ENST00000414678.7:c.3079C= ENSP00000412835.2:p.Gln1027=
ENST00000635849.1:c.2242C= ENSP00000490948.1:p.Gln748=
ENST00000635957.1:c.1873C= ENSP00000490385.1:p.Gln625=
ENST00000636227.1:n.3384C=
ENST00000636254.1:n.841C=
ENST00000636930.2:c.4921C= MANE Select ENSP00000490491.2:p.Gln1641=
ENST00000636940.1:n.2918C=
ENST00000637015.1:c.2289C=
ENST00000637568.1:c.2203C=
ENST00000637741.1:n.1587C=
ENST00000637810.1:c.2263C= ENSP00000489636.1:p.Gln755=
ENST00000637904.1:c.2422C= ENSP00000490550.1:p.Gln808=
ENST00000647938.1:c.4552C= ENSP00000498155.1:p.Gln1518=
ENST00000346085.9:c.4552C= ENSP00000344546.4:p.Gln1518=
ENST00000350026.9:c.4513C= ENSP00000055163.7:p.Gln1505=
ENST00000414678.6:c.3079C= ENSP00000412835.2:p.Gln1027=
NM_017519.2:c.4513C= NP_059989.2:p.Gln1505=
NM_020732.3:c.4552C= NP_065783.3:p.Gln1518=
XM_005267069.3:c.4672C= XP_005267126.2:p.Gln1558=
XM_011535984.1:c.3751C= XP_011534286.1:p.Gln1251=
XM_011535985.1:c.3571C= XP_011534287.1:p.Gln1191=
XM_011535986.1:c.3331C= XP_011534288.1:p.Gln1111=
XM_011535987.1:c.2950C= XP_011534289.1:p.Gln984=
XM_011535988.1:c.1813C= XP_011534290.1:p.Gln605=
NM_001346813.1:c.4672C= NP_001333742.1:p.Gln1558=
NM_001363725.1:c.2422C= NP_001350654.1:p.Gln808=
XM_011535984.2:c.4882C= XP_011534286.2:p.Gln1628=
XM_011535988.3:c.1813C= XP_011534290.1:p.Gln605=
XM_017011103.2:c.4783C= XP_016866592.1:p.Gln1595=
XM_017011104.1:c.4753C= XP_016866593.1:p.Gln1585=
XM_017011105.2:c.4723C= XP_016866594.1:p.Gln1575=
XM_017011106.2:c.4594C= XP_016866595.1:p.Gln1532=
XM_017011107.2:c.4573C= XP_016866596.1:p.Gln1525=
XR_002956289.1:n.4868C=
NM_001363725.2:c.2422C= NP_001350654.1:p.Gln808=
NM_001371656.1:c.4801C= NP_001358585.1:p.Gln1601=
NM_001374820.1:c.4801C= NP_001361749.1:p.Gln1601=
NM_001374828.1:c.4921C= MANE Select NP_001361757.1:p.Gln1641=
NM_017519.3:c.4762C= NP_059989.3:p.Gln1588=