Canonical Allele Identifier: CA1675516904
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148499G= , CM000668.2:g.157148499G= GRCh38
NC_000006.11:g.157469633G= , CM000668.1:g.157469633G= GRCh37
NC_000006.10:g.157511325G= NCBI36
NG_032093.1:g.375570G=
NG_032093.2:g.375570G=
NG_066624.1:g.377474G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.2762-125G= ENSP00000055163.8:n.2762-125G=
ENST00000414678.8:c.2672-125G= ENSP00000412835.3:n.2672-125G=
ENST00000637015.2:c.2762-125G= ENSP00000489729.2:n.2762-125G=
ENST00000319584.11:c.776-125G= ENSP00000313006.7:n.776-125G=
ENST00000346085.10:c.2801-125G= ENSP00000344546.5:n.2801-125G=
ENST00000350026.10:c.2513-125G= ENSP00000055163.7:n.2513-125G=
ENST00000414678.7:c.920-125G= ENSP00000412835.2:n.920-125G=
ENST00000452544.2:n.663-125G=
ENST00000635849.1:c.83-125G= ENSP00000490948.1:n.83-125G=
ENST00000636930.2:c.2762-125G= MANE Select ENSP00000490491.2:n.2762-125G=
ENST00000637810.1:c.263-125G= ENSP00000489636.1:n.263-125G=
ENST00000637904.1:c.263-125G= ENSP00000490550.1:n.263-125G=
ENST00000647938.1:c.2552-125G= ENSP00000498155.1:n.2552-125G=
ENST00000674190.1:n.1511-125G=
ENST00000319584.10:c.779-125G= ENSP00000313006.6:n.779-125G=
ENST00000346085.9:c.2552-125G= ENSP00000344546.4:n.2552-125G=
ENST00000350026.9:c.2513-125G= ENSP00000055163.7:n.2513-125G=
ENST00000414678.6:c.920-125G= ENSP00000412835.2:n.920-125G=
ENST00000452544.1:n.609-125G=
NM_017519.2:c.2513-125G= NP_059989.2:n.2513-125G=
NM_020732.3:c.2552-125G= NP_065783.3:n.2552-125G=
XM_005267069.3:c.2513-125G= XP_005267126.2:n.2513-125G=
XM_011535984.1:c.1463-125G= XP_011534286.1:n.1463-125G=
XM_011535985.1:c.1283-125G= XP_011534287.1:n.1283-125G=
XM_011535986.1:c.1043-125G= XP_011534288.1:n.1043-125G=
XM_011535987.1:c.662-125G= XP_011534289.1:n.662-125G=
XM_011535988.1:c.-20+15292G= XP_011534290.1:n.-20+15292G=
NM_001346813.1:c.2513-125G= NP_001333742.1:n.2513-125G=
NM_001363725.1:c.263-125G= NP_001350654.1:n.263-125G=
XM_011535984.2:c.2594-125G= XP_011534286.2:n.2594-125G=
XM_011535988.3:c.-20+15292G= XP_011534290.1:n.-20+15292G=
XM_017011103.2:c.2594-125G= XP_016866592.1:n.2594-125G=
XM_017011104.1:c.2594-125G= XP_016866593.1:n.2594-125G=
XM_017011105.2:c.2594-125G= XP_016866594.1:n.2594-125G=
XM_017011106.2:c.2594-125G= XP_016866595.1:n.2594-125G=
XM_017011107.2:c.2414-125G= XP_016866596.1:n.2414-125G=
XR_002956289.1:n.2677-125G=
NM_001363725.2:c.263-125G= NP_001350654.1:n.263-125G=
NM_001371656.1:c.2801-125G= NP_001358585.1:n.2801-125G=
NM_001374820.1:c.2801-125G= NP_001361749.1:n.2801-125G=
NM_001374828.1:c.2762-125G= MANE Select NP_001361757.1:n.2762-125G=
NM_017519.3:c.2762-125G= NP_059989.3:n.2762-125G=