Canonical Allele Identifier: CA1675538402
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190099C= , CM000668.2:g.157190099C= GRCh38
NC_000006.11:g.157511233C= , CM000668.1:g.157511233C= GRCh37
NC_000006.10:g.157552925C= NCBI36
NG_032093.1:g.417170C=
NG_032093.2:g.417170C=
NG_066624.1:g.419074C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3961C= ENSP00000055163.8:p.Arg1321=
ENST00000414678.8:c.4030C= ENSP00000412835.3:p.Arg1344=
ENST00000637015.2:c.4249C= ENSP00000489729.2:p.Arg1417=
ENST00000346085.10:c.4000C= ENSP00000344546.5:p.Arg1334=
ENST00000350026.10:c.3712C= ENSP00000055163.7:p.Arg1238=
ENST00000414678.7:c.2278C= ENSP00000412835.2:p.Arg760=
ENST00000635849.1:c.1441C= ENSP00000490948.1:p.Arg481=
ENST00000635957.1:c.1072C= ENSP00000490385.1:p.Arg358=
ENST00000636930.2:c.4120C= MANE Select ENSP00000490491.2:p.Arg1374=
ENST00000636940.1:n.2117C=
ENST00000637015.1:c.1488C=
ENST00000637568.1:c.1402C=
ENST00000637741.1:n.786C=
ENST00000637810.1:c.1462C= ENSP00000489636.1:p.Arg488=
ENST00000637904.1:c.1621C= ENSP00000490550.1:p.Arg541=
ENST00000647938.1:c.3751C= ENSP00000498155.1:p.Arg1251=
ENST00000346085.9:c.3751C= ENSP00000344546.4:p.Arg1251=
ENST00000350026.9:c.3712C= ENSP00000055163.7:p.Arg1238=
ENST00000414678.6:c.2278C= ENSP00000412835.2:p.Arg760=
NM_017519.2:c.3712C= NP_059989.2:p.Arg1238=
NM_020732.3:c.3751C= NP_065783.3:p.Arg1251=
XM_005267069.3:c.3871C= XP_005267126.2:p.Arg1291=
XM_011535984.1:c.2950C= XP_011534286.1:p.Arg984=
XM_011535985.1:c.2770C= XP_011534287.1:p.Arg924=
XM_011535986.1:c.2530C= XP_011534288.1:p.Arg844=
XM_011535987.1:c.2149C= XP_011534289.1:p.Arg717=
XM_011535988.1:c.1012C= XP_011534290.1:p.Arg338=
NM_001346813.1:c.3871C= NP_001333742.1:p.Arg1291=
NM_001363725.1:c.1621C= NP_001350654.1:p.Arg541=
XM_011535984.2:c.4081C= XP_011534286.2:p.Arg1361=
XM_011535988.3:c.1012C= XP_011534290.1:p.Arg338=
XM_017011103.2:c.3982C= XP_016866592.1:p.Arg1328=
XM_017011104.1:c.3952C= XP_016866593.1:p.Arg1318=
XM_017011105.2:c.3922C= XP_016866594.1:p.Arg1308=
XM_017011106.2:c.3793C= XP_016866595.1:p.Arg1265=
XM_017011107.2:c.3772C= XP_016866596.1:p.Arg1258=
XR_002956289.1:n.4164C=
NM_001363725.2:c.1621C= NP_001350654.1:p.Arg541=
NM_001371656.1:c.4000C= NP_001358585.1:p.Arg1334=
NM_001374820.1:c.4000C= NP_001361749.1:p.Arg1334=
NM_001374828.1:c.4120C= MANE Select NP_001361757.1:p.Arg1374=
NM_017519.3:c.3961C= NP_059989.3:p.Arg1321=