Canonical Allele Identifier: CA1675538405
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190105T= , CM000668.2:g.157190105T= GRCh38
NC_000006.11:g.157511239T= , CM000668.1:g.157511239T= GRCh37
NC_000006.10:g.157552931T= NCBI36
NG_032093.1:g.417176T=
NG_032093.2:g.417176T=
NG_066624.1:g.419080T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3967T= ENSP00000055163.8:p.Ser1323=
ENST00000414678.8:c.4036T= ENSP00000412835.3:p.Ser1346=
ENST00000637015.2:c.4255T= ENSP00000489729.2:p.Ser1419=
ENST00000346085.10:c.4006T= ENSP00000344546.5:p.Ser1336=
ENST00000350026.10:c.3718T= ENSP00000055163.7:p.Ser1240=
ENST00000414678.7:c.2284T= ENSP00000412835.2:p.Ser762=
ENST00000635849.1:c.1447T= ENSP00000490948.1:p.Ser483=
ENST00000635957.1:c.1078T= ENSP00000490385.1:p.Ser360=
ENST00000636930.2:c.4126T= MANE Select ENSP00000490491.2:p.Ser1376=
ENST00000636940.1:n.2123T=
ENST00000637015.1:c.1494T=
ENST00000637568.1:c.1408T=
ENST00000637741.1:n.792T=
ENST00000637810.1:c.1468T= ENSP00000489636.1:p.Ser490=
ENST00000637904.1:c.1627T= ENSP00000490550.1:p.Ser543=
ENST00000647938.1:c.3757T= ENSP00000498155.1:p.Ser1253=
ENST00000346085.9:c.3757T= ENSP00000344546.4:p.Ser1253=
ENST00000350026.9:c.3718T= ENSP00000055163.7:p.Ser1240=
ENST00000414678.6:c.2284T= ENSP00000412835.2:p.Ser762=
NM_017519.2:c.3718T= NP_059989.2:p.Ser1240=
NM_020732.3:c.3757T= NP_065783.3:p.Ser1253=
XM_005267069.3:c.3877T= XP_005267126.2:p.Ser1293=
XM_011535984.1:c.2956T= XP_011534286.1:p.Ser986=
XM_011535985.1:c.2776T= XP_011534287.1:p.Ser926=
XM_011535986.1:c.2536T= XP_011534288.1:p.Ser846=
XM_011535987.1:c.2155T= XP_011534289.1:p.Ser719=
XM_011535988.1:c.1018T= XP_011534290.1:p.Ser340=
NM_001346813.1:c.3877T= NP_001333742.1:p.Ser1293=
NM_001363725.1:c.1627T= NP_001350654.1:p.Ser543=
XM_011535984.2:c.4087T= XP_011534286.2:p.Ser1363=
XM_011535988.3:c.1018T= XP_011534290.1:p.Ser340=
XM_017011103.2:c.3988T= XP_016866592.1:p.Ser1330=
XM_017011104.1:c.3958T= XP_016866593.1:p.Ser1320=
XM_017011105.2:c.3928T= XP_016866594.1:p.Ser1310=
XM_017011106.2:c.3799T= XP_016866595.1:p.Ser1267=
XM_017011107.2:c.3778T= XP_016866596.1:p.Ser1260=
XR_002956289.1:n.4170T=
NM_001363725.2:c.1627T= NP_001350654.1:p.Ser543=
NM_001371656.1:c.4006T= NP_001358585.1:p.Ser1336=
NM_001374820.1:c.4006T= NP_001361749.1:p.Ser1336=
NM_001374828.1:c.4126T= MANE Select NP_001361757.1:p.Ser1376=
NM_017519.3:c.3967T= NP_059989.3:p.Ser1323=