Canonical Allele Identifier: CA1675367788
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156829331C= , CM000668.2:g.156829331C= GRCh38
NC_000006.11:g.157150465C= , CM000668.1:g.157150465C= GRCh37
NC_000006.10:g.157192157C= NCBI36
NG_032093.1:g.56402C=
NG_032093.2:g.56402C=
NG_066624.1:g.58306C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.1896C= ENSP00000055163.8:p.Ser632=
ENST00000414678.8:c.1896C= ENSP00000412835.3:p.Ser632=
ENST00000637015.2:c.1896C= ENSP00000489729.2:p.Ser632=
ENST00000346085.10:c.1896C= ENSP00000344546.5:p.Ser632=
ENST00000350026.10:c.1647C= ENSP00000055163.7:p.Ser549=
ENST00000414678.7:c.144C= ENSP00000412835.2:p.Ser48=
ENST00000494260.2:c.177C= ENSP00000490094.1:p.Ser59=
ENST00000636607.1:c.159C= ENSP00000490050.1:p.Ser53=
ENST00000636748.1:c.177C= ENSP00000489917.1:p.Ser59=
ENST00000636930.2:c.1896C= MANE Select ENSP00000490491.2:p.Ser632=
ENST00000637910.1:n.177C=
ENST00000638000.1:c.113C=
ENST00000647938.1:c.1647C= ENSP00000498155.1:p.Ser549=
ENST00000674190.1:n.603C=
ENST00000674298.1:c.1636C=
ENST00000346085.9:c.1647C= ENSP00000344546.4:p.Ser549=
ENST00000350026.9:c.1647C= ENSP00000055163.7:p.Ser549=
ENST00000414678.6:c.144C= ENSP00000412835.2:p.Ser48=
ENST00000494260.1:n.105C=
NM_017519.2:c.1647C= NP_059989.2:p.Ser549=
NM_020732.3:c.1647C= NP_065783.3:p.Ser549=
XM_005267069.3:c.1647C= XP_005267126.2:p.Ser549=
XM_011535984.1:c.516C= XP_011534286.1:p.Ser172=
XM_011535985.1:c.516C= XP_011534287.1:p.Ser172=
XM_011535986.1:c.96C= XP_011534288.1:p.Ser32=
NM_001346813.1:c.1647C= NP_001333742.1:p.Ser549=
XM_011535984.2:c.1647C= XP_011534286.2:p.Ser549=
XM_017011103.2:c.1647C= XP_016866592.1:p.Ser549=
XM_017011104.1:c.1647C= XP_016866593.1:p.Ser549=
XM_017011105.2:c.1647C= XP_016866594.1:p.Ser549=
XM_017011106.2:c.1647C= XP_016866595.1:p.Ser549=
XM_017011107.2:c.1647C= XP_016866596.1:p.Ser549=
XR_002956289.1:n.1730C=
NM_001371656.1:c.1896C= NP_001358585.1:p.Ser632=
NM_001374820.1:c.1896C= NP_001361749.1:p.Ser632=
NM_001374828.1:c.1896C= MANE Select NP_001361757.1:p.Ser632=
NM_017519.3:c.1896C= NP_059989.3:p.Ser632=