Canonical Allele Identifier: CA1675538271
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189767A= , CM000668.2:g.157189767A= GRCh38
NC_000006.11:g.157510901A= , CM000668.1:g.157510901A= GRCh37
NC_000006.10:g.157552593A= NCBI36
NG_032093.1:g.416838A=
NG_032093.2:g.416838A=
NG_066624.1:g.418742A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3886A= ENSP00000055163.8:p.Met1296=
ENST00000414678.8:c.3955A= ENSP00000412835.3:p.Met1319=
ENST00000637015.2:c.4174A= ENSP00000489729.2:p.Met1392=
ENST00000346085.10:c.3925A= ENSP00000344546.5:p.Met1309=
ENST00000350026.10:c.3637A= ENSP00000055163.7:p.Met1213=
ENST00000414678.7:c.2203A= ENSP00000412835.2:p.Met735=
ENST00000635849.1:c.1366A= ENSP00000490948.1:p.Met456=
ENST00000635957.1:c.1000A= ENSP00000490385.1:p.Met334=
ENST00000636930.2:c.4045A= MANE Select ENSP00000490491.2:p.Met1349=
ENST00000636940.1:n.2042A=
ENST00000637015.1:c.1413A=
ENST00000637568.1:c.1327A=
ENST00000637741.1:n.711A=
ENST00000637810.1:c.1387A= ENSP00000489636.1:p.Met463=
ENST00000637904.1:c.1546A= ENSP00000490550.1:p.Met516=
ENST00000647938.1:c.3676A= ENSP00000498155.1:p.Met1226=
ENST00000346085.9:c.3676A= ENSP00000344546.4:p.Met1226=
ENST00000350026.9:c.3637A= ENSP00000055163.7:p.Met1213=
ENST00000414678.6:c.2203A= ENSP00000412835.2:p.Met735=
NM_017519.2:c.3637A= NP_059989.2:p.Met1213=
NM_020732.3:c.3676A= NP_065783.3:p.Met1226=
XM_005267069.3:c.3796A= XP_005267126.2:p.Met1266=
XM_011535984.1:c.2875A= XP_011534286.1:p.Met959=
XM_011535985.1:c.2695A= XP_011534287.1:p.Met899=
XM_011535986.1:c.2455A= XP_011534288.1:p.Met819=
XM_011535987.1:c.2074A= XP_011534289.1:p.Met692=
XM_011535988.1:c.937A= XP_011534290.1:p.Met313=
NM_001346813.1:c.3796A= NP_001333742.1:p.Met1266=
NM_001363725.1:c.1546A= NP_001350654.1:p.Met516=
XM_011535984.2:c.4006A= XP_011534286.2:p.Met1336=
XM_011535988.3:c.937A= XP_011534290.1:p.Met313=
XM_017011103.2:c.3907A= XP_016866592.1:p.Met1303=
XM_017011104.1:c.3877A= XP_016866593.1:p.Met1293=
XM_017011105.2:c.3847A= XP_016866594.1:p.Met1283=
XM_017011106.2:c.3718A= XP_016866595.1:p.Met1240=
XM_017011107.2:c.3697A= XP_016866596.1:p.Met1233=
XR_002956289.1:n.4089A=
NM_001363725.2:c.1546A= NP_001350654.1:p.Met516=
NM_001371656.1:c.3925A= NP_001358585.1:p.Met1309=
NM_001374820.1:c.3925A= NP_001361749.1:p.Met1309=
NM_001374828.1:c.4045A= MANE Select NP_001361757.1:p.Met1349=
NM_017519.3:c.3886A= NP_059989.3:p.Met1296=