Canonical Allele Identifier: CA1675538267

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189755C= , CM000668.2:g.157189755C=	GRCh38
NC_000006.11:g.157510889C= , CM000668.1:g.157510889C=	GRCh37
NC_000006.10:g.157552581C=	NCBI36
NG_032093.1:g.416826C=
NG_032093.2:g.416826C=
NG_066624.1:g.418730C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3874C=	ENSP00000055163.8:p.Gln1292=
ENST00000414678.8:c.3943C=	ENSP00000412835.3:p.Gln1315=
ENST00000637015.2:c.4162C=	ENSP00000489729.2:p.Gln1388=
ENST00000346085.10:c.3913C=	ENSP00000344546.5:p.Gln1305=
ENST00000350026.10:c.3625C=	ENSP00000055163.7:p.Gln1209=
ENST00000414678.7:c.2191C=	ENSP00000412835.2:p.Gln731=
ENST00000635849.1:c.1354C=	ENSP00000490948.1:p.Gln452=
ENST00000635957.1:c.988C=	ENSP00000490385.1:p.Gln330=
ENST00000636930.2:c.4033C= MANE Select	ENSP00000490491.2:p.Gln1345=
ENST00000636940.1:n.2030C=
ENST00000637015.1:c.1401C=
ENST00000637568.1:c.1315C=
ENST00000637741.1:n.699C=
ENST00000637810.1:c.1375C=	ENSP00000489636.1:p.Gln459=
ENST00000637904.1:c.1534C=	ENSP00000490550.1:p.Gln512=
ENST00000647938.1:c.3664C=	ENSP00000498155.1:p.Gln1222=
ENST00000346085.9:c.3664C=	ENSP00000344546.4:p.Gln1222=
ENST00000350026.9:c.3625C=	ENSP00000055163.7:p.Gln1209=
ENST00000414678.6:c.2191C=	ENSP00000412835.2:p.Gln731=
NM_017519.2:c.3625C=	NP_059989.2:p.Gln1209=
NM_020732.3:c.3664C=	NP_065783.3:p.Gln1222=
XM_005267069.3:c.3784C=	XP_005267126.2:p.Gln1262=
XM_011535984.1:c.2863C=	XP_011534286.1:p.Gln955=
XM_011535985.1:c.2683C=	XP_011534287.1:p.Gln895=
XM_011535986.1:c.2443C=	XP_011534288.1:p.Gln815=
XM_011535987.1:c.2062C=	XP_011534289.1:p.Gln688=
XM_011535988.1:c.925C=	XP_011534290.1:p.Gln309=
NM_001346813.1:c.3784C=	NP_001333742.1:p.Gln1262=
NM_001363725.1:c.1534C=	NP_001350654.1:p.Gln512=
XM_011535984.2:c.3994C=	XP_011534286.2:p.Gln1332=
XM_011535988.3:c.925C=	XP_011534290.1:p.Gln309=
XM_017011103.2:c.3895C=	XP_016866592.1:p.Gln1299=
XM_017011104.1:c.3865C=	XP_016866593.1:p.Gln1289=
XM_017011105.2:c.3835C=	XP_016866594.1:p.Gln1279=
XM_017011106.2:c.3706C=	XP_016866595.1:p.Gln1236=
XM_017011107.2:c.3685C=	XP_016866596.1:p.Gln1229=
XR_002956289.1:n.4077C=
NM_001363725.2:c.1534C=	NP_001350654.1:p.Gln512=
NM_001371656.1:c.3913C=	NP_001358585.1:p.Gln1305=
NM_001374820.1:c.3913C=	NP_001361749.1:p.Gln1305=
NM_001374828.1:c.4033C= MANE Select	NP_001361757.1:p.Gln1345=
NM_017519.3:c.3874C=	NP_059989.3:p.Gln1292=