Canonical Allele Identifier: CA1675522797
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157200983T= , CM000668.2:g.157200983T= GRCh38
NC_000006.11:g.157522117T= , CM000668.1:g.157522117T= GRCh37
NC_000006.10:g.157563809T= NCBI36
NG_032093.1:g.428054T=
NG_032093.2:g.428054T=
NG_066624.1:g.429958T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4599T= ENSP00000055163.8:p.Asn1533=
ENST00000414678.8:c.4668T= ENSP00000412835.3:p.Asn1556=
ENST00000637015.2:c.4887T= ENSP00000489729.2:p.Asn1629=
ENST00000346085.10:c.4638T= ENSP00000344546.5:p.Asn1546=
ENST00000350026.10:c.4350T= ENSP00000055163.7:p.Asn1450=
ENST00000414678.7:c.2916T= ENSP00000412835.2:p.Asn972=
ENST00000635849.1:c.2079T= ENSP00000490948.1:p.Asn693=
ENST00000635957.1:c.1710T= ENSP00000490385.1:p.Asn570=
ENST00000636227.1:n.3221T=
ENST00000636254.1:n.678T=
ENST00000636930.2:c.4758T= MANE Select ENSP00000490491.2:p.Asn1586=
ENST00000636940.1:n.2755T=
ENST00000637015.1:c.2126T=
ENST00000637568.1:c.2040T=
ENST00000637741.1:n.1424T=
ENST00000637810.1:c.2100T= ENSP00000489636.1:p.Asn700=
ENST00000637904.1:c.2259T= ENSP00000490550.1:p.Asn753=
ENST00000647938.1:c.4389T= ENSP00000498155.1:p.Asn1463=
ENST00000346085.9:c.4389T= ENSP00000344546.4:p.Asn1463=
ENST00000350026.9:c.4350T= ENSP00000055163.7:p.Asn1450=
ENST00000414678.6:c.2916T= ENSP00000412835.2:p.Asn972=
NM_017519.2:c.4350T= NP_059989.2:p.Asn1450=
NM_020732.3:c.4389T= NP_065783.3:p.Asn1463=
XM_005267069.3:c.4509T= XP_005267126.2:p.Asn1503=
XM_011535984.1:c.3588T= XP_011534286.1:p.Asn1196=
XM_011535985.1:c.3408T= XP_011534287.1:p.Asn1136=
XM_011535986.1:c.3168T= XP_011534288.1:p.Asn1056=
XM_011535987.1:c.2787T= XP_011534289.1:p.Asn929=
XM_011535988.1:c.1650T= XP_011534290.1:p.Asn550=
NM_001346813.1:c.4509T= NP_001333742.1:p.Asn1503=
NM_001363725.1:c.2259T= NP_001350654.1:p.Asn753=
XM_011535984.2:c.4719T= XP_011534286.2:p.Asn1573=
XM_011535988.3:c.1650T= XP_011534290.1:p.Asn550=
XM_017011103.2:c.4620T= XP_016866592.1:p.Asn1540=
XM_017011104.1:c.4590T= XP_016866593.1:p.Asn1530=
XM_017011105.2:c.4560T= XP_016866594.1:p.Asn1520=
XM_017011106.2:c.4431T= XP_016866595.1:p.Asn1477=
XM_017011107.2:c.4410T= XP_016866596.1:p.Asn1470=
XR_002956289.1:n.4705T=
NM_001363725.2:c.2259T= NP_001350654.1:p.Asn753=
NM_001371656.1:c.4638T= NP_001358585.1:p.Asn1546=
NM_001374820.1:c.4638T= NP_001361749.1:p.Asn1546=
NM_001374828.1:c.4758T= MANE Select NP_001361757.1:p.Asn1586=
NM_017519.3:c.4599T= NP_059989.3:p.Asn1533=