Canonical Allele Identifier: CA1675523217
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201244C= , CM000668.2:g.157201244C= GRCh38
NC_000006.11:g.157522378C= , CM000668.1:g.157522378C= GRCh37
NC_000006.10:g.157564070C= NCBI36
NG_032093.1:g.428315C=
NG_032093.2:g.428315C=
NG_066624.1:g.430219C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4860C= ENSP00000055163.8:p.Ile1620=
ENST00000414678.8:c.4929C= ENSP00000412835.3:p.Ile1643=
ENST00000637015.2:c.5148C= ENSP00000489729.2:p.Ile1716=
ENST00000346085.10:c.4899C= ENSP00000344546.5:p.Ile1633=
ENST00000350026.10:c.4611C= ENSP00000055163.7:p.Ile1537=
ENST00000414678.7:c.3177C= ENSP00000412835.2:p.Ile1059=
ENST00000635849.1:c.2340C= ENSP00000490948.1:p.Ile780=
ENST00000635957.1:c.1971C= ENSP00000490385.1:p.Ile657=
ENST00000636227.1:n.3482C=
ENST00000636254.1:n.939C=
ENST00000636930.2:c.5019C= MANE Select ENSP00000490491.2:p.Ile1673=
ENST00000636940.1:n.3016C=
ENST00000637015.1:c.2387C=
ENST00000637568.1:c.2301C=
ENST00000637741.1:n.1685C=
ENST00000637810.1:c.2361C= ENSP00000489636.1:p.Ile787=
ENST00000637904.1:c.2520C= ENSP00000490550.1:p.Ile840=
ENST00000647938.1:c.4650C= ENSP00000498155.1:p.Ile1550=
ENST00000346085.9:c.4650C= ENSP00000344546.4:p.Ile1550=
ENST00000350026.9:c.4611C= ENSP00000055163.7:p.Ile1537=
ENST00000414678.6:c.3177C= ENSP00000412835.2:p.Ile1059=
NM_017519.2:c.4611C= NP_059989.2:p.Ile1537=
NM_020732.3:c.4650C= NP_065783.3:p.Ile1550=
XM_005267069.3:c.4770C= XP_005267126.2:p.Ile1590=
XM_011535984.1:c.3849C= XP_011534286.1:p.Ile1283=
XM_011535985.1:c.3669C= XP_011534287.1:p.Ile1223=
XM_011535986.1:c.3429C= XP_011534288.1:p.Ile1143=
XM_011535987.1:c.3048C= XP_011534289.1:p.Ile1016=
XM_011535988.1:c.1911C= XP_011534290.1:p.Ile637=
NM_001346813.1:c.4770C= NP_001333742.1:p.Ile1590=
NM_001363725.1:c.2520C= NP_001350654.1:p.Ile840=
XM_011535984.2:c.4980C= XP_011534286.2:p.Ile1660=
XM_011535988.3:c.1911C= XP_011534290.1:p.Ile637=
XM_017011103.2:c.4881C= XP_016866592.1:p.Ile1627=
XM_017011104.1:c.4851C= XP_016866593.1:p.Ile1617=
XM_017011105.2:c.4821C= XP_016866594.1:p.Ile1607=
XM_017011106.2:c.4692C= XP_016866595.1:p.Ile1564=
XM_017011107.2:c.4671C= XP_016866596.1:p.Ile1557=
XR_002956289.1:n.4966C=
NM_001363725.2:c.2520C= NP_001350654.1:p.Ile840=
NM_001371656.1:c.4899C= NP_001358585.1:p.Ile1633=
NM_001374820.1:c.4899C= NP_001361749.1:p.Ile1633=
NM_001374828.1:c.5019C= MANE Select NP_001361757.1:p.Ile1673=
NM_017519.3:c.4860C= NP_059989.3:p.Ile1620=