Canonical Allele Identifier: CA1675538409
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190114C= , CM000668.2:g.157190114C= GRCh38
NC_000006.11:g.157511248C= , CM000668.1:g.157511248C= GRCh37
NC_000006.10:g.157552940C= NCBI36
NG_032093.1:g.417185C=
NG_032093.2:g.417185C=
NG_066624.1:g.419089C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3976C= ENSP00000055163.8:p.Pro1326=
ENST00000414678.8:c.4045C= ENSP00000412835.3:p.Pro1349=
ENST00000637015.2:c.4264C= ENSP00000489729.2:p.Pro1422=
ENST00000346085.10:c.4015C= ENSP00000344546.5:p.Pro1339=
ENST00000350026.10:c.3727C= ENSP00000055163.7:p.Pro1243=
ENST00000414678.7:c.2293C= ENSP00000412835.2:p.Pro765=
ENST00000635849.1:c.1456C= ENSP00000490948.1:p.Pro486=
ENST00000635957.1:c.1087C= ENSP00000490385.1:p.Pro363=
ENST00000636930.2:c.4135C= MANE Select ENSP00000490491.2:p.Pro1379=
ENST00000636940.1:n.2132C=
ENST00000637015.1:c.1503C=
ENST00000637568.1:c.1417C=
ENST00000637741.1:n.801C=
ENST00000637810.1:c.1477C= ENSP00000489636.1:p.Pro493=
ENST00000637904.1:c.1636C= ENSP00000490550.1:p.Pro546=
ENST00000647938.1:c.3766C= ENSP00000498155.1:p.Pro1256=
ENST00000346085.9:c.3766C= ENSP00000344546.4:p.Pro1256=
ENST00000350026.9:c.3727C= ENSP00000055163.7:p.Pro1243=
ENST00000414678.6:c.2293C= ENSP00000412835.2:p.Pro765=
NM_017519.2:c.3727C= NP_059989.2:p.Pro1243=
NM_020732.3:c.3766C= NP_065783.3:p.Pro1256=
XM_005267069.3:c.3886C= XP_005267126.2:p.Pro1296=
XM_011535984.1:c.2965C= XP_011534286.1:p.Pro989=
XM_011535985.1:c.2785C= XP_011534287.1:p.Pro929=
XM_011535986.1:c.2545C= XP_011534288.1:p.Pro849=
XM_011535987.1:c.2164C= XP_011534289.1:p.Pro722=
XM_011535988.1:c.1027C= XP_011534290.1:p.Pro343=
NM_001346813.1:c.3886C= NP_001333742.1:p.Pro1296=
NM_001363725.1:c.1636C= NP_001350654.1:p.Pro546=
XM_011535984.2:c.4096C= XP_011534286.2:p.Pro1366=
XM_011535988.3:c.1027C= XP_011534290.1:p.Pro343=
XM_017011103.2:c.3997C= XP_016866592.1:p.Pro1333=
XM_017011104.1:c.3967C= XP_016866593.1:p.Pro1323=
XM_017011105.2:c.3937C= XP_016866594.1:p.Pro1313=
XM_017011106.2:c.3808C= XP_016866595.1:p.Pro1270=
XM_017011107.2:c.3787C= XP_016866596.1:p.Pro1263=
XR_002956289.1:n.4179C=
NM_001363725.2:c.1636C= NP_001350654.1:p.Pro546=
NM_001371656.1:c.4015C= NP_001358585.1:p.Pro1339=
NM_001374820.1:c.4015C= NP_001361749.1:p.Pro1339=
NM_001374828.1:c.4135C= MANE Select NP_001361757.1:p.Pro1379=
NM_017519.3:c.3976C= NP_059989.3:p.Pro1326=