Canonical Allele Identifier: CA1675530508

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206545C= , CM000668.2:g.157206545C=	GRCh38
NC_000006.11:g.157527679C= , CM000668.1:g.157527679C=	GRCh37
NC_000006.10:g.157569371C=	NCBI36
NG_032093.1:g.433616C=
NG_032093.2:g.433616C=
NG_066624.1:g.435520C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5614C=	ENSP00000055163.8:p.Arg1872=
ENST00000414678.8:c.5683C=	ENSP00000412835.3:p.Arg1895=
ENST00000637015.2:c.5902C=	ENSP00000489729.2:p.Arg1968=
ENST00000346085.10:c.5653C=	ENSP00000344546.5:p.Arg1885=
ENST00000350026.10:c.5365C=	ENSP00000055163.7:p.Arg1789=
ENST00000414678.7:c.3931C=	ENSP00000412835.2:p.Arg1311=
ENST00000635849.1:c.3094C=	ENSP00000490948.1:p.Arg1032=
ENST00000635957.1:c.2725C=	ENSP00000490385.1:p.Arg909=
ENST00000636227.1:n.4236C=
ENST00000636254.1:n.1693C=
ENST00000636930.2:c.5773C= MANE Select	ENSP00000490491.2:p.Arg1925=
ENST00000636940.1:n.3770C=
ENST00000637015.1:c.3141C=
ENST00000637568.1:c.3055C=
ENST00000637741.1:n.2439C=
ENST00000637810.1:c.3115C=	ENSP00000489636.1:p.Arg1039=
ENST00000637904.1:c.3274C=	ENSP00000490550.1:p.Arg1092=
ENST00000637933.1:n.2888C=
ENST00000647938.1:c.5404C=	ENSP00000498155.1:p.Arg1802=
ENST00000346085.9:c.5404C=	ENSP00000344546.4:p.Arg1802=
ENST00000350026.9:c.5365C=	ENSP00000055163.7:p.Arg1789=
ENST00000414678.6:c.3931C=	ENSP00000412835.2:p.Arg1311=
NM_017519.2:c.5365C=	NP_059989.2:p.Arg1789=
NM_020732.3:c.5404C=	NP_065783.3:p.Arg1802=
XM_005267069.3:c.5524C=	XP_005267126.2:p.Arg1842=
XM_011535984.1:c.4603C=	XP_011534286.1:p.Arg1535=
XM_011535985.1:c.4423C=	XP_011534287.1:p.Arg1475=
XM_011535986.1:c.4183C=	XP_011534288.1:p.Arg1395=
XM_011535987.1:c.3802C=	XP_011534289.1:p.Arg1268=
XM_011535988.1:c.2665C=	XP_011534290.1:p.Arg889=
NM_001346813.1:c.5524C=	NP_001333742.1:p.Arg1842=
NM_001363725.1:c.3274C=	NP_001350654.1:p.Arg1092=
XM_011535984.2:c.5734C=	XP_011534286.2:p.Arg1912=
XM_011535988.3:c.2665C=	XP_011534290.1:p.Arg889=
XM_017011103.2:c.5635C=	XP_016866592.1:p.Arg1879=
XM_017011104.1:c.5605C=	XP_016866593.1:p.Arg1869=
XM_017011105.2:c.5575C=	XP_016866594.1:p.Arg1859=
XM_017011106.2:c.5446C=	XP_016866595.1:p.Arg1816=
XM_017011107.2:c.5425C=	XP_016866596.1:p.Arg1809=
XR_002956289.1:n.5720C=
NM_001363725.2:c.3274C=	NP_001350654.1:p.Arg1092=
NM_001371656.1:c.5653C=	NP_001358585.1:p.Arg1885=
NM_001374820.1:c.5653C=	NP_001361749.1:p.Arg1885=
NM_001374828.1:c.5773C= MANE Select	NP_001361757.1:p.Arg1925=
NM_017519.3:c.5614C=	NP_059989.3:p.Arg1872=