Canonical Allele Identifier: CA1675522880

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201054C= , CM000668.2:g.157201054C=	GRCh38
NC_000006.11:g.157522188C= , CM000668.1:g.157522188C=	GRCh37
NC_000006.10:g.157563880C=	NCBI36
NG_032093.1:g.428125C=
NG_032093.2:g.428125C=
NG_066624.1:g.430029C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4670C=	ENSP00000055163.8:p.Ala1557=
ENST00000414678.8:c.4739C=	ENSP00000412835.3:p.Ala1580=
ENST00000637015.2:c.4958C=	ENSP00000489729.2:p.Ala1653=
ENST00000346085.10:c.4709C=	ENSP00000344546.5:p.Ala1570=
ENST00000350026.10:c.4421C=	ENSP00000055163.7:p.Ala1474=
ENST00000414678.7:c.2987C=	ENSP00000412835.2:p.Ala996=
ENST00000635849.1:c.2150C=	ENSP00000490948.1:p.Ala717=
ENST00000635957.1:c.1781C=	ENSP00000490385.1:p.Ala594=
ENST00000636227.1:n.3292C=
ENST00000636254.1:n.749C=
ENST00000636930.2:c.4829C= MANE Select	ENSP00000490491.2:p.Ala1610=
ENST00000636940.1:n.2826C=
ENST00000637015.1:c.2197C=
ENST00000637568.1:c.2111C=
ENST00000637741.1:n.1495C=
ENST00000637810.1:c.2171C=	ENSP00000489636.1:p.Ala724=
ENST00000637904.1:c.2330C=	ENSP00000490550.1:p.Ala777=
ENST00000647938.1:c.4460C=	ENSP00000498155.1:p.Ala1487=
ENST00000346085.9:c.4460C=	ENSP00000344546.4:p.Ala1487=
ENST00000350026.9:c.4421C=	ENSP00000055163.7:p.Ala1474=
ENST00000414678.6:c.2987C=	ENSP00000412835.2:p.Ala996=
NM_017519.2:c.4421C=	NP_059989.2:p.Ala1474=
NM_020732.3:c.4460C=	NP_065783.3:p.Ala1487=
XM_005267069.3:c.4580C=	XP_005267126.2:p.Ala1527=
XM_011535984.1:c.3659C=	XP_011534286.1:p.Ala1220=
XM_011535985.1:c.3479C=	XP_011534287.1:p.Ala1160=
XM_011535986.1:c.3239C=	XP_011534288.1:p.Ala1080=
XM_011535987.1:c.2858C=	XP_011534289.1:p.Ala953=
XM_011535988.1:c.1721C=	XP_011534290.1:p.Ala574=
NM_001346813.1:c.4580C=	NP_001333742.1:p.Ala1527=
NM_001363725.1:c.2330C=	NP_001350654.1:p.Ala777=
XM_011535984.2:c.4790C=	XP_011534286.2:p.Ala1597=
XM_011535988.3:c.1721C=	XP_011534290.1:p.Ala574=
XM_017011103.2:c.4691C=	XP_016866592.1:p.Ala1564=
XM_017011104.1:c.4661C=	XP_016866593.1:p.Ala1554=
XM_017011105.2:c.4631C=	XP_016866594.1:p.Ala1544=
XM_017011106.2:c.4502C=	XP_016866595.1:p.Ala1501=
XM_017011107.2:c.4481C=	XP_016866596.1:p.Ala1494=
XR_002956289.1:n.4776C=
NM_001363725.2:c.2330C=	NP_001350654.1:p.Ala777=
NM_001371656.1:c.4709C=	NP_001358585.1:p.Ala1570=
NM_001374820.1:c.4709C=	NP_001361749.1:p.Ala1570=
NM_001374828.1:c.4829C= MANE Select	NP_001361757.1:p.Ala1610=
NM_017519.3:c.4670C=	NP_059989.3:p.Ala1557=