Canonical Allele Identifier: CA1675538412
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190119C= , CM000668.2:g.157190119C= GRCh38
NC_000006.11:g.157511253C= , CM000668.1:g.157511253C= GRCh37
NC_000006.10:g.157552945C= NCBI36
NG_032093.1:g.417190C=
NG_032093.2:g.417190C=
NG_066624.1:g.419094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3981C= ENSP00000055163.8:p.Asn1327=
ENST00000414678.8:c.4050C= ENSP00000412835.3:p.Asn1350=
ENST00000637015.2:c.4269C= ENSP00000489729.2:p.Asn1423=
ENST00000346085.10:c.4020C= ENSP00000344546.5:p.Asn1340=
ENST00000350026.10:c.3732C= ENSP00000055163.7:p.Asn1244=
ENST00000414678.7:c.2298C= ENSP00000412835.2:p.Asn766=
ENST00000635849.1:c.1461C= ENSP00000490948.1:p.Asn487=
ENST00000635957.1:c.1092C= ENSP00000490385.1:p.Asn364=
ENST00000636930.2:c.4140C= MANE Select ENSP00000490491.2:p.Asn1380=
ENST00000636940.1:n.2137C=
ENST00000637015.1:c.1508C=
ENST00000637568.1:c.1422C=
ENST00000637741.1:n.806C=
ENST00000637810.1:c.1482C= ENSP00000489636.1:p.Asn494=
ENST00000637904.1:c.1641C= ENSP00000490550.1:p.Asn547=
ENST00000647938.1:c.3771C= ENSP00000498155.1:p.Asn1257=
ENST00000346085.9:c.3771C= ENSP00000344546.4:p.Asn1257=
ENST00000350026.9:c.3732C= ENSP00000055163.7:p.Asn1244=
ENST00000414678.6:c.2298C= ENSP00000412835.2:p.Asn766=
NM_017519.2:c.3732C= NP_059989.2:p.Asn1244=
NM_020732.3:c.3771C= NP_065783.3:p.Asn1257=
XM_005267069.3:c.3891C= XP_005267126.2:p.Asn1297=
XM_011535984.1:c.2970C= XP_011534286.1:p.Asn990=
XM_011535985.1:c.2790C= XP_011534287.1:p.Asn930=
XM_011535986.1:c.2550C= XP_011534288.1:p.Asn850=
XM_011535987.1:c.2169C= XP_011534289.1:p.Asn723=
XM_011535988.1:c.1032C= XP_011534290.1:p.Asn344=
NM_001346813.1:c.3891C= NP_001333742.1:p.Asn1297=
NM_001363725.1:c.1641C= NP_001350654.1:p.Asn547=
XM_011535984.2:c.4101C= XP_011534286.2:p.Asn1367=
XM_011535988.3:c.1032C= XP_011534290.1:p.Asn344=
XM_017011103.2:c.4002C= XP_016866592.1:p.Asn1334=
XM_017011104.1:c.3972C= XP_016866593.1:p.Asn1324=
XM_017011105.2:c.3942C= XP_016866594.1:p.Asn1314=
XM_017011106.2:c.3813C= XP_016866595.1:p.Asn1271=
XM_017011107.2:c.3792C= XP_016866596.1:p.Asn1264=
XR_002956289.1:n.4184C=
NM_001363725.2:c.1641C= NP_001350654.1:p.Asn547=
NM_001371656.1:c.4020C= NP_001358585.1:p.Asn1340=
NM_001374820.1:c.4020C= NP_001361749.1:p.Asn1340=
NM_001374828.1:c.4140C= MANE Select NP_001361757.1:p.Asn1380=
NM_017519.3:c.3981C= NP_059989.3:p.Asn1327=