Canonical Allele Identifier: CA1675538399
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190094C= , CM000668.2:g.157190094C= GRCh38
NC_000006.11:g.157511228C= , CM000668.1:g.157511228C= GRCh37
NC_000006.10:g.157552920C= NCBI36
NG_032093.1:g.417165C=
NG_032093.2:g.417165C=
NG_066624.1:g.419069C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3956C= ENSP00000055163.8:p.Pro1319=
ENST00000414678.8:c.4025C= ENSP00000412835.3:p.Pro1342=
ENST00000637015.2:c.4244C= ENSP00000489729.2:p.Pro1415=
ENST00000346085.10:c.3995C= ENSP00000344546.5:p.Pro1332=
ENST00000350026.10:c.3707C= ENSP00000055163.7:p.Pro1236=
ENST00000414678.7:c.2273C= ENSP00000412835.2:p.Pro758=
ENST00000635849.1:c.1436C= ENSP00000490948.1:p.Pro479=
ENST00000635957.1:c.1067C= ENSP00000490385.1:p.Pro356=
ENST00000636930.2:c.4115C= MANE Select ENSP00000490491.2:p.Pro1372=
ENST00000636940.1:n.2112C=
ENST00000637015.1:c.1483C=
ENST00000637568.1:c.1397C=
ENST00000637741.1:n.781C=
ENST00000637810.1:c.1457C= ENSP00000489636.1:p.Pro486=
ENST00000637904.1:c.1616C= ENSP00000490550.1:p.Pro539=
ENST00000647938.1:c.3746C= ENSP00000498155.1:p.Pro1249=
ENST00000346085.9:c.3746C= ENSP00000344546.4:p.Pro1249=
ENST00000350026.9:c.3707C= ENSP00000055163.7:p.Pro1236=
ENST00000414678.6:c.2273C= ENSP00000412835.2:p.Pro758=
NM_017519.2:c.3707C= NP_059989.2:p.Pro1236=
NM_020732.3:c.3746C= NP_065783.3:p.Pro1249=
XM_005267069.3:c.3866C= XP_005267126.2:p.Pro1289=
XM_011535984.1:c.2945C= XP_011534286.1:p.Pro982=
XM_011535985.1:c.2765C= XP_011534287.1:p.Pro922=
XM_011535986.1:c.2525C= XP_011534288.1:p.Pro842=
XM_011535987.1:c.2144C= XP_011534289.1:p.Pro715=
XM_011535988.1:c.1007C= XP_011534290.1:p.Pro336=
NM_001346813.1:c.3866C= NP_001333742.1:p.Pro1289=
NM_001363725.1:c.1616C= NP_001350654.1:p.Pro539=
XM_011535984.2:c.4076C= XP_011534286.2:p.Pro1359=
XM_011535988.3:c.1007C= XP_011534290.1:p.Pro336=
XM_017011103.2:c.3977C= XP_016866592.1:p.Pro1326=
XM_017011104.1:c.3947C= XP_016866593.1:p.Pro1316=
XM_017011105.2:c.3917C= XP_016866594.1:p.Pro1306=
XM_017011106.2:c.3788C= XP_016866595.1:p.Pro1263=
XM_017011107.2:c.3767C= XP_016866596.1:p.Pro1256=
XR_002956289.1:n.4159C=
NM_001363725.2:c.1616C= NP_001350654.1:p.Pro539=
NM_001371656.1:c.3995C= NP_001358585.1:p.Pro1332=
NM_001374820.1:c.3995C= NP_001361749.1:p.Pro1332=
NM_001374828.1:c.4115C= MANE Select NP_001361757.1:p.Pro1372=
NM_017519.3:c.3956C= NP_059989.3:p.Pro1319=