Canonical Allele Identifier: CA1675522997
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201114A= , CM000668.2:g.157201114A= GRCh38
NC_000006.11:g.157522248A= , CM000668.1:g.157522248A= GRCh37
NC_000006.10:g.157563940A= NCBI36
NG_032093.1:g.428185A=
NG_032093.2:g.428185A=
NG_066624.1:g.430089A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4730A= ENSP00000055163.8:p.Asn1577=
ENST00000414678.8:c.4799A= ENSP00000412835.3:p.Asn1600=
ENST00000637015.2:c.5018A= ENSP00000489729.2:p.Asn1673=
ENST00000346085.10:c.4769A= ENSP00000344546.5:p.Asn1590=
ENST00000350026.10:c.4481A= ENSP00000055163.7:p.Asn1494=
ENST00000414678.7:c.3047A= ENSP00000412835.2:p.Asn1016=
ENST00000635849.1:c.2210A= ENSP00000490948.1:p.Asn737=
ENST00000635957.1:c.1841A= ENSP00000490385.1:p.Asn614=
ENST00000636227.1:n.3352A=
ENST00000636254.1:n.809A=
ENST00000636930.2:c.4889A= MANE Select ENSP00000490491.2:p.Asn1630=
ENST00000636940.1:n.2886A=
ENST00000637015.1:c.2257A=
ENST00000637568.1:c.2171A=
ENST00000637741.1:n.1555A=
ENST00000637810.1:c.2231A= ENSP00000489636.1:p.Asn744=
ENST00000637904.1:c.2390A= ENSP00000490550.1:p.Asn797=
ENST00000647938.1:c.4520A= ENSP00000498155.1:p.Asn1507=
ENST00000346085.9:c.4520A= ENSP00000344546.4:p.Asn1507=
ENST00000350026.9:c.4481A= ENSP00000055163.7:p.Asn1494=
ENST00000414678.6:c.3047A= ENSP00000412835.2:p.Asn1016=
NM_017519.2:c.4481A= NP_059989.2:p.Asn1494=
NM_020732.3:c.4520A= NP_065783.3:p.Asn1507=
XM_005267069.3:c.4640A= XP_005267126.2:p.Asn1547=
XM_011535984.1:c.3719A= XP_011534286.1:p.Asn1240=
XM_011535985.1:c.3539A= XP_011534287.1:p.Asn1180=
XM_011535986.1:c.3299A= XP_011534288.1:p.Asn1100=
XM_011535987.1:c.2918A= XP_011534289.1:p.Asn973=
XM_011535988.1:c.1781A= XP_011534290.1:p.Asn594=
NM_001346813.1:c.4640A= NP_001333742.1:p.Asn1547=
NM_001363725.1:c.2390A= NP_001350654.1:p.Asn797=
XM_011535984.2:c.4850A= XP_011534286.2:p.Asn1617=
XM_011535988.3:c.1781A= XP_011534290.1:p.Asn594=
XM_017011103.2:c.4751A= XP_016866592.1:p.Asn1584=
XM_017011104.1:c.4721A= XP_016866593.1:p.Asn1574=
XM_017011105.2:c.4691A= XP_016866594.1:p.Asn1564=
XM_017011106.2:c.4562A= XP_016866595.1:p.Asn1521=
XM_017011107.2:c.4541A= XP_016866596.1:p.Asn1514=
XR_002956289.1:n.4836A=
NM_001363725.2:c.2390A= NP_001350654.1:p.Asn797=
NM_001371656.1:c.4769A= NP_001358585.1:p.Asn1590=
NM_001374820.1:c.4769A= NP_001361749.1:p.Asn1590=
NM_001374828.1:c.4889A= MANE Select NP_001361757.1:p.Asn1630=
NM_017519.3:c.4730A= NP_059989.3:p.Asn1577=