Canonical Allele Identifier: CA1675542192
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157198755C= , CM000668.2:g.157198755C= GRCh38
NC_000006.11:g.157519889C= , CM000668.1:g.157519889C= GRCh37
NC_000006.10:g.157561581C= NCBI36
NG_032093.1:g.425826C=
NG_032093.2:g.425826C=
NG_066624.1:g.427730C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4224-56C= ENSP00000055163.8:n.4224-56C=
ENST00000414678.8:c.4293-56C= ENSP00000412835.3:n.4293-56C=
ENST00000637015.2:c.4512-56C= ENSP00000489729.2:n.4512-56C=
ENST00000346085.10:c.4263-56C= ENSP00000344546.5:n.4263-56C=
ENST00000350026.10:c.3975-56C= ENSP00000055163.7:n.3975-56C=
ENST00000414678.7:c.2541-56C= ENSP00000412835.2:n.2541-56C=
ENST00000635849.1:c.1704-56C= ENSP00000490948.1:n.1704-56C=
ENST00000635957.1:c.1335-56C= ENSP00000490385.1:n.1335-56C=
ENST00000636227.1:n.2846-56C=
ENST00000636254.1:n.247C=
ENST00000636930.2:c.4383-56C= MANE Select ENSP00000490491.2:n.4383-56C=
ENST00000636940.1:n.2380-56C=
ENST00000637015.1:c.1751-56C=
ENST00000637568.1:c.1665-56C=
ENST00000637741.1:n.1049-56C=
ENST00000637810.1:c.1725-56C= ENSP00000489636.1:n.1725-56C=
ENST00000637904.1:c.1884-56C= ENSP00000490550.1:n.1884-56C=
ENST00000647938.1:c.4014-56C= ENSP00000498155.1:n.4014-56C=
ENST00000346085.9:c.4014-56C= ENSP00000344546.4:n.4014-56C=
ENST00000350026.9:c.3975-56C= ENSP00000055163.7:n.3975-56C=
ENST00000414678.6:c.2541-56C= ENSP00000412835.2:n.2541-56C=
NM_017519.2:c.3975-56C= NP_059989.2:n.3975-56C=
NM_020732.3:c.4014-56C= NP_065783.3:n.4014-56C=
XM_005267069.3:c.4134-56C= XP_005267126.2:n.4134-56C=
XM_011535984.1:c.3213-56C= XP_011534286.1:n.3213-56C=
XM_011535985.1:c.3033-56C= XP_011534287.1:n.3033-56C=
XM_011535986.1:c.2793-56C= XP_011534288.1:n.2793-56C=
XM_011535987.1:c.2412-56C= XP_011534289.1:n.2412-56C=
XM_011535988.1:c.1275-56C= XP_011534290.1:n.1275-56C=
NM_001346813.1:c.4134-56C= NP_001333742.1:n.4134-56C=
NM_001363725.1:c.1884-56C= NP_001350654.1:n.1884-56C=
XM_011535984.2:c.4344-56C= XP_011534286.2:n.4344-56C=
XM_011535988.3:c.1275-56C= XP_011534290.1:n.1275-56C=
XM_017011103.2:c.4245-56C= XP_016866592.1:n.4245-56C=
XM_017011104.1:c.4215-56C= XP_016866593.1:n.4215-56C=
XM_017011105.2:c.4185-56C= XP_016866594.1:n.4185-56C=
XM_017011106.2:c.4056-56C= XP_016866595.1:n.4056-56C=
XM_017011107.2:c.4035-56C= XP_016866596.1:n.4035-56C=
XR_002956289.1:n.4427-1950C=
NM_001363725.2:c.1884-56C= NP_001350654.1:n.1884-56C=
NM_001371656.1:c.4263-56C= NP_001358585.1:n.4263-56C=
NM_001374820.1:c.4263-56C= NP_001361749.1:n.4263-56C=
NM_001374828.1:c.4383-56C= MANE Select NP_001361757.1:n.4383-56C=
NM_017519.3:c.4224-56C= NP_059989.3:n.4224-56C=