Canonical Allele Identifier: CA16043721
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 374317
dbSNP Id: rs1057518691

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189781G>C , CM000668.2:g.157189781G>C GRCh38
NC_000006.11:g.157510915G>C , CM000668.1:g.157510915G>C GRCh37
NC_000006.10:g.157552607G>C NCBI36
NG_032093.1:g.416852G>C
NG_032093.2:g.416852G>C
NG_066624.1:g.418756G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.3899+1G>C ENSP00000055163.8:n.3899+1G>C
ENST00000414678.8:c.3968+1G>C ENSP00000412835.3:n.3968+1G>C
ENST00000637015.2:c.4187+1G>C ENSP00000489729.2:n.4187+1G>C
ENST00000346085.10:c.3938+1G>C ENSP00000344546.5:n.3938+1G>C
ENST00000350026.10:c.3650+1G>C ENSP00000055163.7:n.3650+1G>C
ENST00000414678.7:c.2216+1G>C ENSP00000412835.2:n.2216+1G>C
ENST00000635849.1:c.1379+1G>C ENSP00000490948.1:n.1379+1G>C
ENST00000635957.1:c.1013+1G>C ENSP00000490385.1:n.1013+1G>C
ENST00000636930.2:c.4058+1G>C MANE Select ENSP00000490491.2:n.4058+1G>C
ENST00000636940.1:n.2055+1G>C
ENST00000637015.1:c.1426+1G>C
ENST00000637568.1:c.1340+1G>C
ENST00000637741.1:n.724+1G>C
ENST00000637810.1:c.1400+1G>C ENSP00000489636.1:n.1400+1G>C
ENST00000637904.1:c.1559+1G>C ENSP00000490550.1:n.1559+1G>C
ENST00000647938.1:c.3689+1G>C ENSP00000498155.1:n.3689+1G>C
ENST00000346085.9:c.3689+1G>C ENSP00000344546.4:n.3689+1G>C
ENST00000350026.9:c.3650+1G>C ENSP00000055163.7:n.3650+1G>C
ENST00000414678.6:c.2216+1G>C ENSP00000412835.2:n.2216+1G>C
NM_017519.2:c.3650+1G>C NP_059989.2:n.3650+1G>C
NM_020732.3:c.3689+1G>C NP_065783.3:n.3689+1G>C
XM_005267069.3:c.3809+1G>C XP_005267126.2:n.3809+1G>C
XM_011535984.1:c.2888+1G>C XP_011534286.1:n.2888+1G>C
XM_011535985.1:c.2708+1G>C XP_011534287.1:n.2708+1G>C
XM_011535986.1:c.2468+1G>C XP_011534288.1:n.2468+1G>C
XM_011535987.1:c.2087+1G>C XP_011534289.1:n.2087+1G>C
XM_011535988.1:c.950+1G>C XP_011534290.1:n.950+1G>C
NM_001346813.1:c.3809+1G>C NP_001333742.1:n.3809+1G>C
NM_001363725.1:c.1559+1G>C NP_001350654.1:n.1559+1G>C
XM_011535984.2:c.4019+1G>C XP_011534286.2:n.4019+1G>C
XM_011535988.3:c.950+1G>C XP_011534290.1:n.950+1G>C
XM_017011103.2:c.3920+1G>C XP_016866592.1:n.3920+1G>C
XM_017011104.1:c.3890+1G>C XP_016866593.1:n.3890+1G>C
XM_017011105.2:c.3860+1G>C XP_016866594.1:n.3860+1G>C
XM_017011106.2:c.3731+1G>C XP_016866595.1:n.3731+1G>C
XM_017011107.2:c.3710+1G>C XP_016866596.1:n.3710+1G>C
XR_002956289.1:n.4102+1G>C
NM_001363725.2:c.1559+1G>C NP_001350654.1:n.1559+1G>C
NM_001371656.1:c.3938+1G>C NP_001358585.1:n.3938+1G>C
NM_001374820.1:c.3938+1G>C NP_001361749.1:n.3938+1G>C
NM_001374828.1:c.4058+1G>C MANE Select NP_001361757.1:n.4058+1G>C
NM_017519.3:c.3899+1G>C NP_059989.3:n.3899+1G>C