Canonical Allele Identifier: CA1675538386
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190055T= , CM000668.2:g.157190055T= GRCh38
NC_000006.11:g.157511189T= , CM000668.1:g.157511189T= GRCh37
NC_000006.10:g.157552881T= NCBI36
NG_032093.1:g.417126T=
NG_032093.2:g.417126T=
NG_066624.1:g.419030T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3917T= ENSP00000055163.8:p.Val1306=
ENST00000414678.8:c.3986T= ENSP00000412835.3:p.Val1329=
ENST00000637015.2:c.4205T= ENSP00000489729.2:p.Val1402=
ENST00000346085.10:c.3956T= ENSP00000344546.5:p.Val1319=
ENST00000350026.10:c.3668T= ENSP00000055163.7:p.Val1223=
ENST00000414678.7:c.2234T= ENSP00000412835.2:p.Val745=
ENST00000635849.1:c.1397T= ENSP00000490948.1:p.Val466=
ENST00000635957.1:c.1028T= ENSP00000490385.1:p.Val343=
ENST00000636930.2:c.4076T= MANE Select ENSP00000490491.2:p.Val1359=
ENST00000636940.1:n.2073T=
ENST00000637015.1:c.1444T=
ENST00000637568.1:c.1358T=
ENST00000637741.1:n.742T=
ENST00000637810.1:c.1418T= ENSP00000489636.1:p.Val473=
ENST00000637904.1:c.1577T= ENSP00000490550.1:p.Val526=
ENST00000647938.1:c.3707T= ENSP00000498155.1:p.Val1236=
ENST00000346085.9:c.3707T= ENSP00000344546.4:p.Val1236=
ENST00000350026.9:c.3668T= ENSP00000055163.7:p.Val1223=
ENST00000414678.6:c.2234T= ENSP00000412835.2:p.Val745=
NM_017519.2:c.3668T= NP_059989.2:p.Val1223=
NM_020732.3:c.3707T= NP_065783.3:p.Val1236=
XM_005267069.3:c.3827T= XP_005267126.2:p.Val1276=
XM_011535984.1:c.2906T= XP_011534286.1:p.Val969=
XM_011535985.1:c.2726T= XP_011534287.1:p.Val909=
XM_011535986.1:c.2486T= XP_011534288.1:p.Val829=
XM_011535987.1:c.2105T= XP_011534289.1:p.Val702=
XM_011535988.1:c.968T= XP_011534290.1:p.Val323=
NM_001346813.1:c.3827T= NP_001333742.1:p.Val1276=
NM_001363725.1:c.1577T= NP_001350654.1:p.Val526=
XM_011535984.2:c.4037T= XP_011534286.2:p.Val1346=
XM_011535988.3:c.968T= XP_011534290.1:p.Val323=
XM_017011103.2:c.3938T= XP_016866592.1:p.Val1313=
XM_017011104.1:c.3908T= XP_016866593.1:p.Val1303=
XM_017011105.2:c.3878T= XP_016866594.1:p.Val1293=
XM_017011106.2:c.3749T= XP_016866595.1:p.Val1250=
XM_017011107.2:c.3728T= XP_016866596.1:p.Val1243=
XR_002956289.1:n.4120T=
NM_001363725.2:c.1577T= NP_001350654.1:p.Val526=
NM_001371656.1:c.3956T= NP_001358585.1:p.Val1319=
NM_001374820.1:c.3956T= NP_001361749.1:p.Val1319=
NM_001374828.1:c.4076T= MANE Select NP_001361757.1:p.Val1359=
NM_017519.3:c.3917T= NP_059989.3:p.Val1306=