Canonical Allele Identifier: CA1675535765
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184312A= , CM000668.2:g.157184312A= GRCh38
NC_000006.11:g.157505446A= , CM000668.1:g.157505446A= GRCh37
NC_000006.10:g.157547138A= NCBI36
NG_032093.1:g.411383A=
NG_032093.2:g.411383A=
NG_066624.1:g.413287A=

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.3637A= ENSP00000055163.8:p.Lys1213=
ENST00000414678.8:c.3706A= ENSP00000412835.3:p.Lys1236=
ENST00000637015.2:c.3925A= ENSP00000489729.2:p.Lys1309=
ENST00000319584.11:c.1810A= ENSP00000313006.7:p.Lys604=
ENST00000346085.10:c.3676A= ENSP00000344546.5:p.Lys1226=
ENST00000350026.10:c.3388A= ENSP00000055163.7:p.Lys1130=
ENST00000414678.7:c.1954A= ENSP00000412835.2:p.Lys652=
ENST00000635849.1:c.1117A= ENSP00000490948.1:p.Lys373=
ENST00000635957.1:c.751A= ENSP00000490385.1:p.Lys251=
ENST00000636930.2:c.3796A= MANE Select ENSP00000490491.2:p.Lys1266=
ENST00000636940.1:n.1793A=
ENST00000637015.1:c.1164A=
ENST00000637568.1:c.1078A=
ENST00000637741.1:n.462A=
ENST00000637810.1:c.1138A= ENSP00000489636.1:p.Lys380=
ENST00000637904.1:c.1297A= ENSP00000490550.1:p.Lys433=
ENST00000647938.1:c.3427A= ENSP00000498155.1:p.Lys1143=
ENST00000319584.10:c.1813A= ENSP00000313006.6:p.Lys605=
ENST00000346085.9:c.3427A= ENSP00000344546.4:p.Lys1143=
ENST00000350026.9:c.3388A= ENSP00000055163.7:p.Lys1130=
ENST00000400790.3:c.589A= ENSP00000383596.3:p.Lys197=
ENST00000414678.6:c.1954A= ENSP00000412835.2:p.Lys652=
NM_017519.2:c.3388A= NP_059989.2:p.Lys1130=
NM_020732.3:c.3427A= NP_065783.3:p.Lys1143=
XM_005267069.3:c.3547A= XP_005267126.2:p.Lys1183=
XM_011535984.1:c.2626A= XP_011534286.1:p.Lys876=
XM_011535985.1:c.2446A= XP_011534287.1:p.Lys816=
XM_011535986.1:c.2206A= XP_011534288.1:p.Lys736=
XM_011535987.1:c.1825A= XP_011534289.1:p.Lys609=
XM_011535988.1:c.688A= XP_011534290.1:p.Lys230=
NM_001346813.1:c.3547A= NP_001333742.1:p.Lys1183=
NM_001363725.1:c.1297A= NP_001350654.1:p.Lys433=
XM_011535984.2:c.3757A= XP_011534286.2:p.Lys1253=
XM_011535988.3:c.688A= XP_011534290.1:p.Lys230=
XM_017011103.2:c.3658A= XP_016866592.1:p.Lys1220=
XM_017011104.1:c.3628A= XP_016866593.1:p.Lys1210=
XM_017011105.2:c.3598A= XP_016866594.1:p.Lys1200=
XM_017011106.2:c.3469A= XP_016866595.1:p.Lys1157=
XM_017011107.2:c.3448A= XP_016866596.1:p.Lys1150=
XR_002956289.1:n.3840A=
NM_001363725.2:c.1297A= NP_001350654.1:p.Lys433=
NM_001371656.1:c.3676A= NP_001358585.1:p.Lys1226=
NM_001374820.1:c.3676A= NP_001361749.1:p.Lys1226=
NM_001374828.1:c.3796A= MANE Select NP_001361757.1:p.Lys1266=
NM_017519.3:c.3637A= NP_059989.3:p.Lys1213=