Canonical Allele Identifier: CA366381308
Gene: ARID1B HGNC NCBI

Linked Data

dbSNP Id: rs1371991750

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778119C>A , CM000668.2:g.156778119C>A GRCh38
NC_000006.11:g.157099253C>A , CM000668.1:g.157099253C>A GRCh37
NC_000006.10:g.157140945C>A NCBI36
NG_032093.1:g.5190C>A
NG_032093.2:g.5190C>A
NG_066624.1:g.7094C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.439C>A ENSP00000055163.8:p.Leu147Ile
ENST00000414678.8:c.439C>A ENSP00000412835.3:p.Leu147Ile
ENST00000637015.2:c.439C>A ENSP00000489729.2:p.Leu147Ile
ENST00000346085.10:c.439C>A ENSP00000344546.5:p.Leu147Ile
ENST00000350026.10:c.190C>A ENSP00000055163.7:p.Leu64Ile
ENST00000636930.2:c.439C>A MANE Select ENSP00000490491.2:p.Leu147Ile
ENST00000647938.1:c.190C>A ENSP00000498155.1:p.Leu64Ile
ENST00000674298.1:c.179C>A
ENST00000346085.9:c.190C>A ENSP00000344546.4:p.Leu64Ile
ENST00000350026.9:c.190C>A ENSP00000055163.7:p.Leu64Ile
NM_017519.2:c.190C>A NP_059989.2:p.Leu64Ile
NM_020732.3:c.190C>A NP_065783.3:p.Leu64Ile
XM_005267069.3:c.190C>A XP_005267126.2:p.Leu64Ile
XR_943148.1:n.177+127G>T
NM_001346813.1:c.190C>A NP_001333742.1:p.Leu64Ile
XM_011535984.2:c.190C>A XP_011534286.2:p.Leu64Ile
XM_017011103.2:c.190C>A XP_016866592.1:p.Leu64Ile
XM_017011104.1:c.190C>A XP_016866593.1:p.Leu64Ile
XM_017011105.2:c.190C>A XP_016866594.1:p.Leu64Ile
XM_017011106.2:c.190C>A XP_016866595.1:p.Leu64Ile
XM_017011107.2:c.190C>A XP_016866596.1:p.Leu64Ile
XR_002956289.1:n.273C>A
NM_001371656.1:c.439C>A NP_001358585.1:p.Leu147Ile
NM_001374820.1:c.439C>A NP_001361749.1:p.Leu147Ile
NM_001374828.1:c.439C>A MANE Select NP_001361757.1:p.Leu147Ile
NM_017519.3:c.439C>A NP_059989.3:p.Leu147Ile
NR_163974.1:n.273+127G>T