Canonical Allele Identifier: CA1675538414
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190122C= , CM000668.2:g.157190122C= GRCh38
NC_000006.11:g.157511256C= , CM000668.1:g.157511256C= GRCh37
NC_000006.10:g.157552948C= NCBI36
NG_032093.1:g.417193C=
NG_032093.2:g.417193C=
NG_066624.1:g.419097C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3984C= ENSP00000055163.8:p.Ala1328=
ENST00000414678.8:c.4053C= ENSP00000412835.3:p.Ala1351=
ENST00000637015.2:c.4272C= ENSP00000489729.2:p.Ala1424=
ENST00000346085.10:c.4023C= ENSP00000344546.5:p.Ala1341=
ENST00000350026.10:c.3735C= ENSP00000055163.7:p.Ala1245=
ENST00000414678.7:c.2301C= ENSP00000412835.2:p.Ala767=
ENST00000635849.1:c.1464C= ENSP00000490948.1:p.Ala488=
ENST00000635957.1:c.1095C= ENSP00000490385.1:p.Ala365=
ENST00000636930.2:c.4143C= MANE Select ENSP00000490491.2:p.Ala1381=
ENST00000636940.1:n.2140C=
ENST00000637015.1:c.1511C=
ENST00000637568.1:c.1425C=
ENST00000637741.1:n.809C=
ENST00000637810.1:c.1485C= ENSP00000489636.1:p.Ala495=
ENST00000637904.1:c.1644C= ENSP00000490550.1:p.Ala548=
ENST00000647938.1:c.3774C= ENSP00000498155.1:p.Ala1258=
ENST00000346085.9:c.3774C= ENSP00000344546.4:p.Ala1258=
ENST00000350026.9:c.3735C= ENSP00000055163.7:p.Ala1245=
ENST00000414678.6:c.2301C= ENSP00000412835.2:p.Ala767=
NM_017519.2:c.3735C= NP_059989.2:p.Ala1245=
NM_020732.3:c.3774C= NP_065783.3:p.Ala1258=
XM_005267069.3:c.3894C= XP_005267126.2:p.Ala1298=
XM_011535984.1:c.2973C= XP_011534286.1:p.Ala991=
XM_011535985.1:c.2793C= XP_011534287.1:p.Ala931=
XM_011535986.1:c.2553C= XP_011534288.1:p.Ala851=
XM_011535987.1:c.2172C= XP_011534289.1:p.Ala724=
XM_011535988.1:c.1035C= XP_011534290.1:p.Ala345=
NM_001346813.1:c.3894C= NP_001333742.1:p.Ala1298=
NM_001363725.1:c.1644C= NP_001350654.1:p.Ala548=
XM_011535984.2:c.4104C= XP_011534286.2:p.Ala1368=
XM_011535988.3:c.1035C= XP_011534290.1:p.Ala345=
XM_017011103.2:c.4005C= XP_016866592.1:p.Ala1335=
XM_017011104.1:c.3975C= XP_016866593.1:p.Ala1325=
XM_017011105.2:c.3945C= XP_016866594.1:p.Ala1315=
XM_017011106.2:c.3816C= XP_016866595.1:p.Ala1272=
XM_017011107.2:c.3795C= XP_016866596.1:p.Ala1265=
XR_002956289.1:n.4187C=
NM_001363725.2:c.1644C= NP_001350654.1:p.Ala548=
NM_001371656.1:c.4023C= NP_001358585.1:p.Ala1341=
NM_001374820.1:c.4023C= NP_001361749.1:p.Ala1341=
NM_001374828.1:c.4143C= MANE Select NP_001361757.1:p.Ala1381=
NM_017519.3:c.3984C= NP_059989.3:p.Ala1328=