Canonical Allele Identifier: CA1675538263
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189749C= , CM000668.2:g.157189749C= GRCh38
NC_000006.11:g.157510883C= , CM000668.1:g.157510883C= GRCh37
NC_000006.10:g.157552575C= NCBI36
NG_032093.1:g.416820C=
NG_032093.2:g.416820C=
NG_066624.1:g.418724C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3868C= ENSP00000055163.8:p.His1290=
ENST00000414678.8:c.3937C= ENSP00000412835.3:p.His1313=
ENST00000637015.2:c.4156C= ENSP00000489729.2:p.His1386=
ENST00000346085.10:c.3907C= ENSP00000344546.5:p.His1303=
ENST00000350026.10:c.3619C= ENSP00000055163.7:p.His1207=
ENST00000414678.7:c.2185C= ENSP00000412835.2:p.His729=
ENST00000635849.1:c.1348C= ENSP00000490948.1:p.His450=
ENST00000635957.1:c.982C= ENSP00000490385.1:p.His328=
ENST00000636930.2:c.4027C= MANE Select ENSP00000490491.2:p.His1343=
ENST00000636940.1:n.2024C=
ENST00000637015.1:c.1395C=
ENST00000637568.1:c.1309C=
ENST00000637741.1:n.693C=
ENST00000637810.1:c.1369C= ENSP00000489636.1:p.His457=
ENST00000637904.1:c.1528C= ENSP00000490550.1:p.His510=
ENST00000647938.1:c.3658C= ENSP00000498155.1:p.His1220=
ENST00000346085.9:c.3658C= ENSP00000344546.4:p.His1220=
ENST00000350026.9:c.3619C= ENSP00000055163.7:p.His1207=
ENST00000414678.6:c.2185C= ENSP00000412835.2:p.His729=
NM_017519.2:c.3619C= NP_059989.2:p.His1207=
NM_020732.3:c.3658C= NP_065783.3:p.His1220=
XM_005267069.3:c.3778C= XP_005267126.2:p.His1260=
XM_011535984.1:c.2857C= XP_011534286.1:p.His953=
XM_011535985.1:c.2677C= XP_011534287.1:p.His893=
XM_011535986.1:c.2437C= XP_011534288.1:p.His813=
XM_011535987.1:c.2056C= XP_011534289.1:p.His686=
XM_011535988.1:c.919C= XP_011534290.1:p.His307=
NM_001346813.1:c.3778C= NP_001333742.1:p.His1260=
NM_001363725.1:c.1528C= NP_001350654.1:p.His510=
XM_011535984.2:c.3988C= XP_011534286.2:p.His1330=
XM_011535988.3:c.919C= XP_011534290.1:p.His307=
XM_017011103.2:c.3889C= XP_016866592.1:p.His1297=
XM_017011104.1:c.3859C= XP_016866593.1:p.His1287=
XM_017011105.2:c.3829C= XP_016866594.1:p.His1277=
XM_017011106.2:c.3700C= XP_016866595.1:p.His1234=
XM_017011107.2:c.3679C= XP_016866596.1:p.His1227=
XR_002956289.1:n.4071C=
NM_001363725.2:c.1528C= NP_001350654.1:p.His510=
NM_001371656.1:c.3907C= NP_001358585.1:p.His1303=
NM_001374820.1:c.3907C= NP_001361749.1:p.His1303=
NM_001374828.1:c.4027C= MANE Select NP_001361757.1:p.His1343=
NM_017519.3:c.3868C= NP_059989.3:p.His1290=