Canonical Allele Identifier: CA1675538410
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190116A= , CM000668.2:g.157190116A= GRCh38
NC_000006.11:g.157511250A= , CM000668.1:g.157511250A= GRCh37
NC_000006.10:g.157552942A= NCBI36
NG_032093.1:g.417187A=
NG_032093.2:g.417187A=
NG_066624.1:g.419091A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3978A= ENSP00000055163.8:p.Pro1326=
ENST00000414678.8:c.4047A= ENSP00000412835.3:p.Pro1349=
ENST00000637015.2:c.4266A= ENSP00000489729.2:p.Pro1422=
ENST00000346085.10:c.4017A= ENSP00000344546.5:p.Pro1339=
ENST00000350026.10:c.3729A= ENSP00000055163.7:p.Pro1243=
ENST00000414678.7:c.2295A= ENSP00000412835.2:p.Pro765=
ENST00000635849.1:c.1458A= ENSP00000490948.1:p.Pro486=
ENST00000635957.1:c.1089A= ENSP00000490385.1:p.Pro363=
ENST00000636930.2:c.4137A= MANE Select ENSP00000490491.2:p.Pro1379=
ENST00000636940.1:n.2134A=
ENST00000637015.1:c.1505A=
ENST00000637568.1:c.1419A=
ENST00000637741.1:n.803A=
ENST00000637810.1:c.1479A= ENSP00000489636.1:p.Pro493=
ENST00000637904.1:c.1638A= ENSP00000490550.1:p.Pro546=
ENST00000647938.1:c.3768A= ENSP00000498155.1:p.Pro1256=
ENST00000346085.9:c.3768A= ENSP00000344546.4:p.Pro1256=
ENST00000350026.9:c.3729A= ENSP00000055163.7:p.Pro1243=
ENST00000414678.6:c.2295A= ENSP00000412835.2:p.Pro765=
NM_017519.2:c.3729A= NP_059989.2:p.Pro1243=
NM_020732.3:c.3768A= NP_065783.3:p.Pro1256=
XM_005267069.3:c.3888A= XP_005267126.2:p.Pro1296=
XM_011535984.1:c.2967A= XP_011534286.1:p.Pro989=
XM_011535985.1:c.2787A= XP_011534287.1:p.Pro929=
XM_011535986.1:c.2547A= XP_011534288.1:p.Pro849=
XM_011535987.1:c.2166A= XP_011534289.1:p.Pro722=
XM_011535988.1:c.1029A= XP_011534290.1:p.Pro343=
NM_001346813.1:c.3888A= NP_001333742.1:p.Pro1296=
NM_001363725.1:c.1638A= NP_001350654.1:p.Pro546=
XM_011535984.2:c.4098A= XP_011534286.2:p.Pro1366=
XM_011535988.3:c.1029A= XP_011534290.1:p.Pro343=
XM_017011103.2:c.3999A= XP_016866592.1:p.Pro1333=
XM_017011104.1:c.3969A= XP_016866593.1:p.Pro1323=
XM_017011105.2:c.3939A= XP_016866594.1:p.Pro1313=
XM_017011106.2:c.3810A= XP_016866595.1:p.Pro1270=
XM_017011107.2:c.3789A= XP_016866596.1:p.Pro1263=
XR_002956289.1:n.4181A=
NM_001363725.2:c.1638A= NP_001350654.1:p.Pro546=
NM_001371656.1:c.4017A= NP_001358585.1:p.Pro1339=
NM_001374820.1:c.4017A= NP_001361749.1:p.Pro1339=
NM_001374828.1:c.4137A= MANE Select NP_001361757.1:p.Pro1379=
NM_017519.3:c.3978A= NP_059989.3:p.Pro1326=