Canonical Allele Identifier: CA16618266
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 418864
ClinVar RCV Id: RCV000478760
dbSNP Id: rs1064793482

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201050C>T , CM000668.2:g.157201050C>T GRCh38
NC_000006.11:g.157522184C>T , CM000668.1:g.157522184C>T GRCh37
NC_000006.10:g.157563876C>T NCBI36
NG_032093.1:g.428121C>T
NG_032093.2:g.428121C>T
NG_066624.1:g.430025C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.4666C>T ENSP00000055163.8:p.Gln1556Ter
ENST00000414678.8:c.4735C>T ENSP00000412835.3:p.Gln1579Ter
ENST00000637015.2:c.4954C>T ENSP00000489729.2:p.Gln1652Ter
ENST00000346085.10:c.4705C>T ENSP00000344546.5:p.Gln1569Ter
ENST00000350026.10:c.4417C>T ENSP00000055163.7:p.Gln1473Ter
ENST00000414678.7:c.2983C>T ENSP00000412835.2:p.Gln995Ter
ENST00000635849.1:c.2146C>T ENSP00000490948.1:p.Gln716Ter
ENST00000635957.1:c.1777C>T ENSP00000490385.1:p.Gln593Ter
ENST00000636227.1:n.3288C>T
ENST00000636254.1:n.745C>T
ENST00000636930.2:c.4825C>T MANE Select ENSP00000490491.2:p.Gln1609Ter
ENST00000636940.1:n.2822C>T
ENST00000637015.1:c.2193C>T
ENST00000637568.1:c.2107C>T
ENST00000637741.1:n.1491C>T
ENST00000637810.1:c.2167C>T ENSP00000489636.1:p.Gln723Ter
ENST00000637904.1:c.2326C>T ENSP00000490550.1:p.Gln776Ter
ENST00000647938.1:c.4456C>T ENSP00000498155.1:p.Gln1486Ter
ENST00000346085.9:c.4456C>T ENSP00000344546.4:p.Gln1486Ter
ENST00000350026.9:c.4417C>T ENSP00000055163.7:p.Gln1473Ter
ENST00000414678.6:c.2983C>T ENSP00000412835.2:p.Gln995Ter
NM_017519.2:c.4417C>T NP_059989.2:p.Gln1473Ter
NM_020732.3:c.4456C>T NP_065783.3:p.Gln1486Ter
XM_005267069.3:c.4576C>T XP_005267126.2:p.Gln1526Ter
XM_011535984.1:c.3655C>T XP_011534286.1:p.Gln1219Ter
XM_011535985.1:c.3475C>T XP_011534287.1:p.Gln1159Ter
XM_011535986.1:c.3235C>T XP_011534288.1:p.Gln1079Ter
XM_011535987.1:c.2854C>T XP_011534289.1:p.Gln952Ter
XM_011535988.1:c.1717C>T XP_011534290.1:p.Gln573Ter
NM_001346813.1:c.4576C>T NP_001333742.1:p.Gln1526Ter
NM_001363725.1:c.2326C>T NP_001350654.1:p.Gln776Ter
XM_011535984.2:c.4786C>T XP_011534286.2:p.Gln1596Ter
XM_011535988.3:c.1717C>T XP_011534290.1:p.Gln573Ter
XM_017011103.2:c.4687C>T XP_016866592.1:p.Gln1563Ter
XM_017011104.1:c.4657C>T XP_016866593.1:p.Gln1553Ter
XM_017011105.2:c.4627C>T XP_016866594.1:p.Gln1543Ter
XM_017011106.2:c.4498C>T XP_016866595.1:p.Gln1500Ter
XM_017011107.2:c.4477C>T XP_016866596.1:p.Gln1493Ter
XR_002956289.1:n.4772C>T
NM_001363725.2:c.2326C>T NP_001350654.1:p.Gln776Ter
NM_001371656.1:c.4705C>T NP_001358585.1:p.Gln1569Ter
NM_001374820.1:c.4705C>T NP_001361749.1:p.Gln1569Ter
NM_001374828.1:c.4825C>T MANE Select NP_001361757.1:p.Gln1609Ter
NM_017519.3:c.4666C>T NP_059989.3:p.Gln1556Ter