Canonical Allele Identifier: CA1675538232

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189669A= , CM000668.2:g.157189669A=	GRCh38
NC_000006.11:g.157510803A= , CM000668.1:g.157510803A=	GRCh37
NC_000006.10:g.157552495A=	NCBI36
NG_032093.1:g.416740A=
NG_032093.2:g.416740A=
NG_066624.1:g.418644A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3788A=	ENSP00000055163.8:p.Gln1263=
ENST00000414678.8:c.3857A=	ENSP00000412835.3:p.Gln1286=
ENST00000637015.2:c.4076A=	ENSP00000489729.2:p.Gln1359=
ENST00000346085.10:c.3827A=	ENSP00000344546.5:p.Gln1276=
ENST00000350026.10:c.3539A=	ENSP00000055163.7:p.Gln1180=
ENST00000414678.7:c.2105A=	ENSP00000412835.2:p.Gln702=
ENST00000635849.1:c.1268A=	ENSP00000490948.1:p.Gln423=
ENST00000635957.1:c.902A=	ENSP00000490385.1:p.Gln301=
ENST00000636930.2:c.3947A= MANE Select	ENSP00000490491.2:p.Gln1316=
ENST00000636940.1:n.1944A=
ENST00000637015.1:c.1315A=
ENST00000637568.1:c.1229A=
ENST00000637741.1:n.613A=
ENST00000637810.1:c.1289A=	ENSP00000489636.1:p.Gln430=
ENST00000637904.1:c.1448A=	ENSP00000490550.1:p.Gln483=
ENST00000647938.1:c.3578A=	ENSP00000498155.1:p.Gln1193=
ENST00000346085.9:c.3578A=	ENSP00000344546.4:p.Gln1193=
ENST00000350026.9:c.3539A=	ENSP00000055163.7:p.Gln1180=
ENST00000414678.6:c.2105A=	ENSP00000412835.2:p.Gln702=
NM_017519.2:c.3539A=	NP_059989.2:p.Gln1180=
NM_020732.3:c.3578A=	NP_065783.3:p.Gln1193=
XM_005267069.3:c.3698A=	XP_005267126.2:p.Gln1233=
XM_011535984.1:c.2777A=	XP_011534286.1:p.Gln926=
XM_011535985.1:c.2597A=	XP_011534287.1:p.Gln866=
XM_011535986.1:c.2357A=	XP_011534288.1:p.Gln786=
XM_011535987.1:c.1976A=	XP_011534289.1:p.Gln659=
XM_011535988.1:c.839A=	XP_011534290.1:p.Gln280=
NM_001346813.1:c.3698A=	NP_001333742.1:p.Gln1233=
NM_001363725.1:c.1448A=	NP_001350654.1:p.Gln483=
XM_011535984.2:c.3908A=	XP_011534286.2:p.Gln1303=
XM_011535988.3:c.839A=	XP_011534290.1:p.Gln280=
XM_017011103.2:c.3809A=	XP_016866592.1:p.Gln1270=
XM_017011104.1:c.3779A=	XP_016866593.1:p.Gln1260=
XM_017011105.2:c.3749A=	XP_016866594.1:p.Gln1250=
XM_017011106.2:c.3620A=	XP_016866595.1:p.Gln1207=
XM_017011107.2:c.3599A=	XP_016866596.1:p.Gln1200=
XR_002956289.1:n.3991A=
NM_001363725.2:c.1448A=	NP_001350654.1:p.Gln483=
NM_001371656.1:c.3827A=	NP_001358585.1:p.Gln1276=
NM_001374820.1:c.3827A=	NP_001361749.1:p.Gln1276=
NM_001374828.1:c.3947A= MANE Select	NP_001361757.1:p.Gln1316=
NM_017519.3:c.3788A=	NP_059989.3:p.Gln1263=