Canonical Allele Identifier: CA1675538392
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190066T= , CM000668.2:g.157190066T= GRCh38
NC_000006.11:g.157511200T= , CM000668.1:g.157511200T= GRCh37
NC_000006.10:g.157552892T= NCBI36
NG_032093.1:g.417137T=
NG_032093.2:g.417137T=
NG_066624.1:g.419041T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3928T= ENSP00000055163.8:p.Phe1310=
ENST00000414678.8:c.3997T= ENSP00000412835.3:p.Phe1333=
ENST00000637015.2:c.4216T= ENSP00000489729.2:p.Phe1406=
ENST00000346085.10:c.3967T= ENSP00000344546.5:p.Phe1323=
ENST00000350026.10:c.3679T= ENSP00000055163.7:p.Phe1227=
ENST00000414678.7:c.2245T= ENSP00000412835.2:p.Phe749=
ENST00000635849.1:c.1408T= ENSP00000490948.1:p.Phe470=
ENST00000635957.1:c.1039T= ENSP00000490385.1:p.Phe347=
ENST00000636930.2:c.4087T= MANE Select ENSP00000490491.2:p.Phe1363=
ENST00000636940.1:n.2084T=
ENST00000637015.1:c.1455T=
ENST00000637568.1:c.1369T=
ENST00000637741.1:n.753T=
ENST00000637810.1:c.1429T= ENSP00000489636.1:p.Phe477=
ENST00000637904.1:c.1588T= ENSP00000490550.1:p.Phe530=
ENST00000647938.1:c.3718T= ENSP00000498155.1:p.Phe1240=
ENST00000346085.9:c.3718T= ENSP00000344546.4:p.Phe1240=
ENST00000350026.9:c.3679T= ENSP00000055163.7:p.Phe1227=
ENST00000414678.6:c.2245T= ENSP00000412835.2:p.Phe749=
NM_017519.2:c.3679T= NP_059989.2:p.Phe1227=
NM_020732.3:c.3718T= NP_065783.3:p.Phe1240=
XM_005267069.3:c.3838T= XP_005267126.2:p.Phe1280=
XM_011535984.1:c.2917T= XP_011534286.1:p.Phe973=
XM_011535985.1:c.2737T= XP_011534287.1:p.Phe913=
XM_011535986.1:c.2497T= XP_011534288.1:p.Phe833=
XM_011535987.1:c.2116T= XP_011534289.1:p.Phe706=
XM_011535988.1:c.979T= XP_011534290.1:p.Phe327=
NM_001346813.1:c.3838T= NP_001333742.1:p.Phe1280=
NM_001363725.1:c.1588T= NP_001350654.1:p.Phe530=
XM_011535984.2:c.4048T= XP_011534286.2:p.Phe1350=
XM_011535988.3:c.979T= XP_011534290.1:p.Phe327=
XM_017011103.2:c.3949T= XP_016866592.1:p.Phe1317=
XM_017011104.1:c.3919T= XP_016866593.1:p.Phe1307=
XM_017011105.2:c.3889T= XP_016866594.1:p.Phe1297=
XM_017011106.2:c.3760T= XP_016866595.1:p.Phe1254=
XM_017011107.2:c.3739T= XP_016866596.1:p.Phe1247=
XR_002956289.1:n.4131T=
NM_001363725.2:c.1588T= NP_001350654.1:p.Phe530=
NM_001371656.1:c.3967T= NP_001358585.1:p.Phe1323=
NM_001374820.1:c.3967T= NP_001361749.1:p.Phe1323=
NM_001374828.1:c.4087T= MANE Select NP_001361757.1:p.Phe1363=
NM_017519.3:c.3928T= NP_059989.3:p.Phe1310=