Canonical Allele Identifier: CA1675522995
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201113A= , CM000668.2:g.157201113A= GRCh38
NC_000006.11:g.157522247A= , CM000668.1:g.157522247A= GRCh37
NC_000006.10:g.157563939A= NCBI36
NG_032093.1:g.428184A=
NG_032093.2:g.428184A=
NG_066624.1:g.430088A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4729A= ENSP00000055163.8:p.Asn1577=
ENST00000414678.8:c.4798A= ENSP00000412835.3:p.Asn1600=
ENST00000637015.2:c.5017A= ENSP00000489729.2:p.Asn1673=
ENST00000346085.10:c.4768A= ENSP00000344546.5:p.Asn1590=
ENST00000350026.10:c.4480A= ENSP00000055163.7:p.Asn1494=
ENST00000414678.7:c.3046A= ENSP00000412835.2:p.Asn1016=
ENST00000635849.1:c.2209A= ENSP00000490948.1:p.Asn737=
ENST00000635957.1:c.1840A= ENSP00000490385.1:p.Asn614=
ENST00000636227.1:n.3351A=
ENST00000636254.1:n.808A=
ENST00000636930.2:c.4888A= MANE Select ENSP00000490491.2:p.Asn1630=
ENST00000636940.1:n.2885A=
ENST00000637015.1:c.2256A=
ENST00000637568.1:c.2170A=
ENST00000637741.1:n.1554A=
ENST00000637810.1:c.2230A= ENSP00000489636.1:p.Asn744=
ENST00000637904.1:c.2389A= ENSP00000490550.1:p.Asn797=
ENST00000647938.1:c.4519A= ENSP00000498155.1:p.Asn1507=
ENST00000346085.9:c.4519A= ENSP00000344546.4:p.Asn1507=
ENST00000350026.9:c.4480A= ENSP00000055163.7:p.Asn1494=
ENST00000414678.6:c.3046A= ENSP00000412835.2:p.Asn1016=
NM_017519.2:c.4480A= NP_059989.2:p.Asn1494=
NM_020732.3:c.4519A= NP_065783.3:p.Asn1507=
XM_005267069.3:c.4639A= XP_005267126.2:p.Asn1547=
XM_011535984.1:c.3718A= XP_011534286.1:p.Asn1240=
XM_011535985.1:c.3538A= XP_011534287.1:p.Asn1180=
XM_011535986.1:c.3298A= XP_011534288.1:p.Asn1100=
XM_011535987.1:c.2917A= XP_011534289.1:p.Asn973=
XM_011535988.1:c.1780A= XP_011534290.1:p.Asn594=
NM_001346813.1:c.4639A= NP_001333742.1:p.Asn1547=
NM_001363725.1:c.2389A= NP_001350654.1:p.Asn797=
XM_011535984.2:c.4849A= XP_011534286.2:p.Asn1617=
XM_011535988.3:c.1780A= XP_011534290.1:p.Asn594=
XM_017011103.2:c.4750A= XP_016866592.1:p.Asn1584=
XM_017011104.1:c.4720A= XP_016866593.1:p.Asn1574=
XM_017011105.2:c.4690A= XP_016866594.1:p.Asn1564=
XM_017011106.2:c.4561A= XP_016866595.1:p.Asn1521=
XM_017011107.2:c.4540A= XP_016866596.1:p.Asn1514=
XR_002956289.1:n.4835A=
NM_001363725.2:c.2389A= NP_001350654.1:p.Asn797=
NM_001371656.1:c.4768A= NP_001358585.1:p.Asn1590=
NM_001374820.1:c.4768A= NP_001361749.1:p.Asn1590=
NM_001374828.1:c.4888A= MANE Select NP_001361757.1:p.Asn1630=
NM_017519.3:c.4729A= NP_059989.3:p.Asn1577=