Canonical Allele Identifier: CA1675506546
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157133100C= , CM000668.2:g.157133100C= GRCh38
NC_000006.11:g.157454234C= , CM000668.1:g.157454234C= GRCh37
NC_000006.10:g.157495926C= NCBI36
NG_032093.1:g.360171C=
NG_032093.2:g.360171C=
NG_066624.1:g.362075C=

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.2654C= MANE Select NP_001361757.1:p.Ser885=
ENST00000636930.2:c.2654C= MANE Select ENSP00000490491.2:p.Ser885=
NM_001346813.1:c.2405C= NP_001333742.1:p.Ser802=
NM_001363725.1:c.155C= NP_001350654.1:p.Ser52=
NM_001363725.2:c.155C= NP_001350654.1:p.Ser52=
NM_001371656.1:c.2693C= NP_001358585.1:p.Ser898=
NM_001374820.1:c.2693C= NP_001361749.1:p.Ser898=
NM_017519.2:c.2405C= NP_059989.2:p.Ser802=
NM_017519.3:c.2654C= NP_059989.3:p.Ser885=
NM_020732.3:c.2444C= NP_065783.3:p.Ser815=
ENST00000319584.10:c.671C= ENSP00000313006.6:p.Ser224=
ENST00000319584.11:c.668C= ENSP00000313006.7:p.Ser223=
ENST00000346085.10:c.2693C= ENSP00000344546.5:p.Ser898=
ENST00000346085.9:c.2444C= ENSP00000344546.4:p.Ser815=
ENST00000350026.10:c.2405C= ENSP00000055163.7:p.Ser802=
ENST00000350026.11:c.2654C= ENSP00000055163.8:p.Ser885=
ENST00000350026.9:c.2405C= ENSP00000055163.7:p.Ser802=
ENST00000414678.6:c.812C= ENSP00000412835.2:p.Ser271=
ENST00000414678.7:c.812C= ENSP00000412835.2:p.Ser271=
ENST00000414678.8:c.2564C= ENSP00000412835.3:p.Ser855=
ENST00000452544.1:n.501C=
ENST00000452544.2:n.555C=
ENST00000635849.1:c.83-15524C= ENSP00000490948.1:n.83-15524C=
ENST00000637003.1:c.155C= ENSP00000489666.1:p.Ser52=
ENST00000637015.2:c.2654C= ENSP00000489729.2:p.Ser885=
ENST00000637810.1:c.155C= ENSP00000489636.1:p.Ser52=
ENST00000637904.1:c.155C= ENSP00000490550.1:p.Ser52=
ENST00000647938.1:c.2444C= ENSP00000498155.1:p.Ser815=
ENST00000674190.1:n.1403C=
XM_005267069.3:c.2405C= XP_005267126.2:p.Ser802=
XM_011535984.1:c.1355C= XP_011534286.1:p.Ser452=
XM_011535984.2:c.2486C= XP_011534286.2:p.Ser829=
XM_011535985.1:c.1283-15524C= XP_011534287.1:n.1283-15524C=
XM_011535986.1:c.935C= XP_011534288.1:p.Ser312=
XM_011535987.1:c.554C= XP_011534289.1:p.Ser185=
XM_017011103.2:c.2486C= XP_016866592.1:p.Ser829=
XM_017011104.1:c.2486C= XP_016866593.1:p.Ser829=
XM_017011105.2:c.2486C= XP_016866594.1:p.Ser829=
XM_017011106.2:c.2486C= XP_016866595.1:p.Ser829=
XM_017011107.2:c.2414-15524C= XP_016866596.1:n.2414-15524C=
XR_002956289.1:n.2569C=