Canonical Allele Identifier: CA1675538415
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190124C= , CM000668.2:g.157190124C= GRCh38
NC_000006.11:g.157511258C= , CM000668.1:g.157511258C= GRCh37
NC_000006.10:g.157552950C= NCBI36
NG_032093.1:g.417195C=
NG_032093.2:g.417195C=
NG_066624.1:g.419099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3986C= ENSP00000055163.8:p.Pro1329=
ENST00000414678.8:c.4055C= ENSP00000412835.3:p.Pro1352=
ENST00000637015.2:c.4274C= ENSP00000489729.2:p.Pro1425=
ENST00000346085.10:c.4025C= ENSP00000344546.5:p.Pro1342=
ENST00000350026.10:c.3737C= ENSP00000055163.7:p.Pro1246=
ENST00000414678.7:c.2303C= ENSP00000412835.2:p.Pro768=
ENST00000635849.1:c.1466C= ENSP00000490948.1:p.Pro489=
ENST00000635957.1:c.1097C= ENSP00000490385.1:p.Pro366=
ENST00000636930.2:c.4145C= MANE Select ENSP00000490491.2:p.Pro1382=
ENST00000636940.1:n.2142C=
ENST00000637015.1:c.1513C=
ENST00000637568.1:c.1427C=
ENST00000637741.1:n.811C=
ENST00000637810.1:c.1487C= ENSP00000489636.1:p.Pro496=
ENST00000637904.1:c.1646C= ENSP00000490550.1:p.Pro549=
ENST00000647938.1:c.3776C= ENSP00000498155.1:p.Pro1259=
ENST00000346085.9:c.3776C= ENSP00000344546.4:p.Pro1259=
ENST00000350026.9:c.3737C= ENSP00000055163.7:p.Pro1246=
ENST00000414678.6:c.2303C= ENSP00000412835.2:p.Pro768=
NM_017519.2:c.3737C= NP_059989.2:p.Pro1246=
NM_020732.3:c.3776C= NP_065783.3:p.Pro1259=
XM_005267069.3:c.3896C= XP_005267126.2:p.Pro1299=
XM_011535984.1:c.2975C= XP_011534286.1:p.Pro992=
XM_011535985.1:c.2795C= XP_011534287.1:p.Pro932=
XM_011535986.1:c.2555C= XP_011534288.1:p.Pro852=
XM_011535987.1:c.2174C= XP_011534289.1:p.Pro725=
XM_011535988.1:c.1037C= XP_011534290.1:p.Pro346=
NM_001346813.1:c.3896C= NP_001333742.1:p.Pro1299=
NM_001363725.1:c.1646C= NP_001350654.1:p.Pro549=
XM_011535984.2:c.4106C= XP_011534286.2:p.Pro1369=
XM_011535988.3:c.1037C= XP_011534290.1:p.Pro346=
XM_017011103.2:c.4007C= XP_016866592.1:p.Pro1336=
XM_017011104.1:c.3977C= XP_016866593.1:p.Pro1326=
XM_017011105.2:c.3947C= XP_016866594.1:p.Pro1316=
XM_017011106.2:c.3818C= XP_016866595.1:p.Pro1273=
XM_017011107.2:c.3797C= XP_016866596.1:p.Pro1266=
XR_002956289.1:n.4189C=
NM_001363725.2:c.1646C= NP_001350654.1:p.Pro549=
NM_001371656.1:c.4025C= NP_001358585.1:p.Pro1342=
NM_001374820.1:c.4025C= NP_001361749.1:p.Pro1342=
NM_001374828.1:c.4145C= MANE Select NP_001361757.1:p.Pro1382=
NM_017519.3:c.3986C= NP_059989.3:p.Pro1329=