Canonical Allele Identifier: CA1675538230
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189666C= , CM000668.2:g.157189666C= GRCh38
NC_000006.11:g.157510800C= , CM000668.1:g.157510800C= GRCh37
NC_000006.10:g.157552492C= NCBI36
NG_032093.1:g.416737C=
NG_032093.2:g.416737C=
NG_066624.1:g.418641C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3785C= ENSP00000055163.8:p.Pro1262=
ENST00000414678.8:c.3854C= ENSP00000412835.3:p.Pro1285=
ENST00000637015.2:c.4073C= ENSP00000489729.2:p.Pro1358=
ENST00000346085.10:c.3824C= ENSP00000344546.5:p.Pro1275=
ENST00000350026.10:c.3536C= ENSP00000055163.7:p.Pro1179=
ENST00000414678.7:c.2102C= ENSP00000412835.2:p.Pro701=
ENST00000635849.1:c.1265C= ENSP00000490948.1:p.Pro422=
ENST00000635957.1:c.899C= ENSP00000490385.1:p.Pro300=
ENST00000636930.2:c.3944C= MANE Select ENSP00000490491.2:p.Pro1315=
ENST00000636940.1:n.1941C=
ENST00000637015.1:c.1312C=
ENST00000637568.1:c.1226C=
ENST00000637741.1:n.610C=
ENST00000637810.1:c.1286C= ENSP00000489636.1:p.Pro429=
ENST00000637904.1:c.1445C= ENSP00000490550.1:p.Pro482=
ENST00000647938.1:c.3575C= ENSP00000498155.1:p.Pro1192=
ENST00000346085.9:c.3575C= ENSP00000344546.4:p.Pro1192=
ENST00000350026.9:c.3536C= ENSP00000055163.7:p.Pro1179=
ENST00000414678.6:c.2102C= ENSP00000412835.2:p.Pro701=
NM_017519.2:c.3536C= NP_059989.2:p.Pro1179=
NM_020732.3:c.3575C= NP_065783.3:p.Pro1192=
XM_005267069.3:c.3695C= XP_005267126.2:p.Pro1232=
XM_011535984.1:c.2774C= XP_011534286.1:p.Pro925=
XM_011535985.1:c.2594C= XP_011534287.1:p.Pro865=
XM_011535986.1:c.2354C= XP_011534288.1:p.Pro785=
XM_011535987.1:c.1973C= XP_011534289.1:p.Pro658=
XM_011535988.1:c.836C= XP_011534290.1:p.Pro279=
NM_001346813.1:c.3695C= NP_001333742.1:p.Pro1232=
NM_001363725.1:c.1445C= NP_001350654.1:p.Pro482=
XM_011535984.2:c.3905C= XP_011534286.2:p.Pro1302=
XM_011535988.3:c.836C= XP_011534290.1:p.Pro279=
XM_017011103.2:c.3806C= XP_016866592.1:p.Pro1269=
XM_017011104.1:c.3776C= XP_016866593.1:p.Pro1259=
XM_017011105.2:c.3746C= XP_016866594.1:p.Pro1249=
XM_017011106.2:c.3617C= XP_016866595.1:p.Pro1206=
XM_017011107.2:c.3596C= XP_016866596.1:p.Pro1199=
XR_002956289.1:n.3988C=
NM_001363725.2:c.1445C= NP_001350654.1:p.Pro482=
NM_001371656.1:c.3824C= NP_001358585.1:p.Pro1275=
NM_001374820.1:c.3824C= NP_001361749.1:p.Pro1275=
NM_001374828.1:c.3944C= MANE Select NP_001361757.1:p.Pro1315=
NM_017519.3:c.3785C= NP_059989.3:p.Pro1262=