Canonical Allele Identifier: CA1675538401
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190096A= , CM000668.2:g.157190096A= GRCh38
NC_000006.11:g.157511230A= , CM000668.1:g.157511230A= GRCh37
NC_000006.10:g.157552922A= NCBI36
NG_032093.1:g.417167A=
NG_032093.2:g.417167A=
NG_066624.1:g.419071A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3958A= ENSP00000055163.8:p.Lys1320=
ENST00000414678.8:c.4027A= ENSP00000412835.3:p.Lys1343=
ENST00000637015.2:c.4246A= ENSP00000489729.2:p.Lys1416=
ENST00000346085.10:c.3997A= ENSP00000344546.5:p.Lys1333=
ENST00000350026.10:c.3709A= ENSP00000055163.7:p.Lys1237=
ENST00000414678.7:c.2275A= ENSP00000412835.2:p.Lys759=
ENST00000635849.1:c.1438A= ENSP00000490948.1:p.Lys480=
ENST00000635957.1:c.1069A= ENSP00000490385.1:p.Lys357=
ENST00000636930.2:c.4117A= MANE Select ENSP00000490491.2:p.Lys1373=
ENST00000636940.1:n.2114A=
ENST00000637015.1:c.1485A=
ENST00000637568.1:c.1399A=
ENST00000637741.1:n.783A=
ENST00000637810.1:c.1459A= ENSP00000489636.1:p.Lys487=
ENST00000637904.1:c.1618A= ENSP00000490550.1:p.Lys540=
ENST00000647938.1:c.3748A= ENSP00000498155.1:p.Lys1250=
ENST00000346085.9:c.3748A= ENSP00000344546.4:p.Lys1250=
ENST00000350026.9:c.3709A= ENSP00000055163.7:p.Lys1237=
ENST00000414678.6:c.2275A= ENSP00000412835.2:p.Lys759=
NM_017519.2:c.3709A= NP_059989.2:p.Lys1237=
NM_020732.3:c.3748A= NP_065783.3:p.Lys1250=
XM_005267069.3:c.3868A= XP_005267126.2:p.Lys1290=
XM_011535984.1:c.2947A= XP_011534286.1:p.Lys983=
XM_011535985.1:c.2767A= XP_011534287.1:p.Lys923=
XM_011535986.1:c.2527A= XP_011534288.1:p.Lys843=
XM_011535987.1:c.2146A= XP_011534289.1:p.Lys716=
XM_011535988.1:c.1009A= XP_011534290.1:p.Lys337=
NM_001346813.1:c.3868A= NP_001333742.1:p.Lys1290=
NM_001363725.1:c.1618A= NP_001350654.1:p.Lys540=
XM_011535984.2:c.4078A= XP_011534286.2:p.Lys1360=
XM_011535988.3:c.1009A= XP_011534290.1:p.Lys337=
XM_017011103.2:c.3979A= XP_016866592.1:p.Lys1327=
XM_017011104.1:c.3949A= XP_016866593.1:p.Lys1317=
XM_017011105.2:c.3919A= XP_016866594.1:p.Lys1307=
XM_017011106.2:c.3790A= XP_016866595.1:p.Lys1264=
XM_017011107.2:c.3769A= XP_016866596.1:p.Lys1257=
XR_002956289.1:n.4161A=
NM_001363725.2:c.1618A= NP_001350654.1:p.Lys540=
NM_001371656.1:c.3997A= NP_001358585.1:p.Lys1333=
NM_001374820.1:c.3997A= NP_001361749.1:p.Lys1333=
NM_001374828.1:c.4117A= MANE Select NP_001361757.1:p.Lys1373=
NM_017519.3:c.3958A= NP_059989.3:p.Lys1320=