Canonical Allele Identifier: CA366382859
Gene: ARID1B HGNC NCBI

Linked Data

dbSNP Id: rs1778885433

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778708G>A , CM000668.2:g.156778708G>A GRCh38
NC_000006.11:g.157099842G>A , CM000668.1:g.157099842G>A GRCh37
NC_000006.10:g.157141534G>A NCBI36
NG_032093.1:g.5779G>A
NG_032093.2:g.5779G>A
NG_066624.1:g.7683G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.1028G>A ENSP00000055163.8:p.Ser343Asn
ENST00000414678.8:c.1028G>A ENSP00000412835.3:p.Ser343Asn
ENST00000637015.2:c.1028G>A ENSP00000489729.2:p.Ser343Asn
ENST00000346085.10:c.1028G>A ENSP00000344546.5:p.Ser343Asn
ENST00000350026.10:c.779G>A ENSP00000055163.7:p.Ser260Asn
ENST00000636930.2:c.1028G>A MANE Select ENSP00000490491.2:p.Ser343Asn
ENST00000647938.1:c.779G>A ENSP00000498155.1:p.Ser260Asn
ENST00000674298.1:c.768G>A
ENST00000346085.9:c.779G>A ENSP00000344546.4:p.Ser260Asn
ENST00000350026.9:c.779G>A ENSP00000055163.7:p.Ser260Asn
NM_017519.2:c.779G>A NP_059989.2:p.Ser260Asn
NM_020732.3:c.779G>A NP_065783.3:p.Ser260Asn
XM_005267069.3:c.779G>A XP_005267126.2:p.Ser260Asn
NM_001346813.1:c.779G>A NP_001333742.1:p.Ser260Asn
XM_011535984.2:c.779G>A XP_011534286.2:p.Ser260Asn
XM_017011103.2:c.779G>A XP_016866592.1:p.Ser260Asn
XM_017011104.1:c.779G>A XP_016866593.1:p.Ser260Asn
XM_017011105.2:c.779G>A XP_016866594.1:p.Ser260Asn
XM_017011106.2:c.779G>A XP_016866595.1:p.Ser260Asn
XM_017011107.2:c.779G>A XP_016866596.1:p.Ser260Asn
XR_002956289.1:n.862G>A
NM_001371656.1:c.1028G>A NP_001358585.1:p.Ser343Asn
NM_001374820.1:c.1028G>A NP_001361749.1:p.Ser343Asn
NM_001374828.1:c.1028G>A MANE Select NP_001361757.1:p.Ser343Asn
NM_017519.3:c.1028G>A NP_059989.3:p.Ser343Asn