Canonical Allele Identifier: CA1675538407
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190108A= , CM000668.2:g.157190108A= GRCh38
NC_000006.11:g.157511242A= , CM000668.1:g.157511242A= GRCh37
NC_000006.10:g.157552934A= NCBI36
NG_032093.1:g.417179A=
NG_032093.2:g.417179A=
NG_066624.1:g.419083A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3970A= ENSP00000055163.8:p.Met1324=
ENST00000414678.8:c.4039A= ENSP00000412835.3:p.Met1347=
ENST00000637015.2:c.4258A= ENSP00000489729.2:p.Met1420=
ENST00000346085.10:c.4009A= ENSP00000344546.5:p.Met1337=
ENST00000350026.10:c.3721A= ENSP00000055163.7:p.Met1241=
ENST00000414678.7:c.2287A= ENSP00000412835.2:p.Met763=
ENST00000635849.1:c.1450A= ENSP00000490948.1:p.Met484=
ENST00000635957.1:c.1081A= ENSP00000490385.1:p.Met361=
ENST00000636930.2:c.4129A= MANE Select ENSP00000490491.2:p.Met1377=
ENST00000636940.1:n.2126A=
ENST00000637015.1:c.1497A=
ENST00000637568.1:c.1411A=
ENST00000637741.1:n.795A=
ENST00000637810.1:c.1471A= ENSP00000489636.1:p.Met491=
ENST00000637904.1:c.1630A= ENSP00000490550.1:p.Met544=
ENST00000647938.1:c.3760A= ENSP00000498155.1:p.Met1254=
ENST00000346085.9:c.3760A= ENSP00000344546.4:p.Met1254=
ENST00000350026.9:c.3721A= ENSP00000055163.7:p.Met1241=
ENST00000414678.6:c.2287A= ENSP00000412835.2:p.Met763=
NM_017519.2:c.3721A= NP_059989.2:p.Met1241=
NM_020732.3:c.3760A= NP_065783.3:p.Met1254=
XM_005267069.3:c.3880A= XP_005267126.2:p.Met1294=
XM_011535984.1:c.2959A= XP_011534286.1:p.Met987=
XM_011535985.1:c.2779A= XP_011534287.1:p.Met927=
XM_011535986.1:c.2539A= XP_011534288.1:p.Met847=
XM_011535987.1:c.2158A= XP_011534289.1:p.Met720=
XM_011535988.1:c.1021A= XP_011534290.1:p.Met341=
NM_001346813.1:c.3880A= NP_001333742.1:p.Met1294=
NM_001363725.1:c.1630A= NP_001350654.1:p.Met544=
XM_011535984.2:c.4090A= XP_011534286.2:p.Met1364=
XM_011535988.3:c.1021A= XP_011534290.1:p.Met341=
XM_017011103.2:c.3991A= XP_016866592.1:p.Met1331=
XM_017011104.1:c.3961A= XP_016866593.1:p.Met1321=
XM_017011105.2:c.3931A= XP_016866594.1:p.Met1311=
XM_017011106.2:c.3802A= XP_016866595.1:p.Met1268=
XM_017011107.2:c.3781A= XP_016866596.1:p.Met1261=
XR_002956289.1:n.4173A=
NM_001363725.2:c.1630A= NP_001350654.1:p.Met544=
NM_001371656.1:c.4009A= NP_001358585.1:p.Met1337=
NM_001374820.1:c.4009A= NP_001361749.1:p.Met1337=
NM_001374828.1:c.4129A= MANE Select NP_001361757.1:p.Met1377=
NM_017519.3:c.3970A= NP_059989.3:p.Met1324=