Canonical Allele Identifier: CA1675538382
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190046C= , CM000668.2:g.157190046C= GRCh38
NC_000006.11:g.157511180C= , CM000668.1:g.157511180C= GRCh37
NC_000006.10:g.157552872C= NCBI36
NG_032093.1:g.417117C=
NG_032093.2:g.417117C=
NG_066624.1:g.419021C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3908C= ENSP00000055163.8:p.Thr1303=
ENST00000414678.8:c.3977C= ENSP00000412835.3:p.Thr1326=
ENST00000637015.2:c.4196C= ENSP00000489729.2:p.Thr1399=
ENST00000346085.10:c.3947C= ENSP00000344546.5:p.Thr1316=
ENST00000350026.10:c.3659C= ENSP00000055163.7:p.Thr1220=
ENST00000414678.7:c.2225C= ENSP00000412835.2:p.Thr742=
ENST00000635849.1:c.1388C= ENSP00000490948.1:p.Thr463=
ENST00000635957.1:c.1019C= ENSP00000490385.1:p.Thr340=
ENST00000636930.2:c.4067C= MANE Select ENSP00000490491.2:p.Thr1356=
ENST00000636940.1:n.2064C=
ENST00000637015.1:c.1435C=
ENST00000637568.1:c.1349C=
ENST00000637741.1:n.733C=
ENST00000637810.1:c.1409C= ENSP00000489636.1:p.Thr470=
ENST00000637904.1:c.1568C= ENSP00000490550.1:p.Thr523=
ENST00000647938.1:c.3698C= ENSP00000498155.1:p.Thr1233=
ENST00000346085.9:c.3698C= ENSP00000344546.4:p.Thr1233=
ENST00000350026.9:c.3659C= ENSP00000055163.7:p.Thr1220=
ENST00000414678.6:c.2225C= ENSP00000412835.2:p.Thr742=
NM_017519.2:c.3659C= NP_059989.2:p.Thr1220=
NM_020732.3:c.3698C= NP_065783.3:p.Thr1233=
XM_005267069.3:c.3818C= XP_005267126.2:p.Thr1273=
XM_011535984.1:c.2897C= XP_011534286.1:p.Thr966=
XM_011535985.1:c.2717C= XP_011534287.1:p.Thr906=
XM_011535986.1:c.2477C= XP_011534288.1:p.Thr826=
XM_011535987.1:c.2096C= XP_011534289.1:p.Thr699=
XM_011535988.1:c.959C= XP_011534290.1:p.Thr320=
NM_001346813.1:c.3818C= NP_001333742.1:p.Thr1273=
NM_001363725.1:c.1568C= NP_001350654.1:p.Thr523=
XM_011535984.2:c.4028C= XP_011534286.2:p.Thr1343=
XM_011535988.3:c.959C= XP_011534290.1:p.Thr320=
XM_017011103.2:c.3929C= XP_016866592.1:p.Thr1310=
XM_017011104.1:c.3899C= XP_016866593.1:p.Thr1300=
XM_017011105.2:c.3869C= XP_016866594.1:p.Thr1290=
XM_017011106.2:c.3740C= XP_016866595.1:p.Thr1247=
XM_017011107.2:c.3719C= XP_016866596.1:p.Thr1240=
XR_002956289.1:n.4111C=
NM_001363725.2:c.1568C= NP_001350654.1:p.Thr523=
NM_001371656.1:c.3947C= NP_001358585.1:p.Thr1316=
NM_001374820.1:c.3947C= NP_001361749.1:p.Thr1316=
NM_001374828.1:c.4067C= MANE Select NP_001361757.1:p.Thr1356=
NM_017519.3:c.3908C= NP_059989.3:p.Thr1303=