Canonical Allele Identifier: CA1675523069

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201154G= , CM000668.2:g.157201154G=	GRCh38
NC_000006.11:g.157522288G= , CM000668.1:g.157522288G=	GRCh37
NC_000006.10:g.157563980G=	NCBI36
NG_032093.1:g.428225G=
NG_032093.2:g.428225G=
NG_066624.1:g.430129G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4770G=	ENSP00000055163.8:p.Gln1590=
ENST00000414678.8:c.4839G=	ENSP00000412835.3:p.Gln1613=
ENST00000637015.2:c.5058G=	ENSP00000489729.2:p.Gln1686=
ENST00000346085.10:c.4809G=	ENSP00000344546.5:p.Gln1603=
ENST00000350026.10:c.4521G=	ENSP00000055163.7:p.Gln1507=
ENST00000414678.7:c.3087G=	ENSP00000412835.2:p.Gln1029=
ENST00000635849.1:c.2250G=	ENSP00000490948.1:p.Gln750=
ENST00000635957.1:c.1881G=	ENSP00000490385.1:p.Gln627=
ENST00000636227.1:n.3392G=
ENST00000636254.1:n.849G=
ENST00000636930.2:c.4929G= MANE Select	ENSP00000490491.2:p.Gln1643=
ENST00000636940.1:n.2926G=
ENST00000637015.1:c.2297G=
ENST00000637568.1:c.2211G=
ENST00000637741.1:n.1595G=
ENST00000637810.1:c.2271G=	ENSP00000489636.1:p.Gln757=
ENST00000637904.1:c.2430G=	ENSP00000490550.1:p.Gln810=
ENST00000647938.1:c.4560G=	ENSP00000498155.1:p.Gln1520=
ENST00000346085.9:c.4560G=	ENSP00000344546.4:p.Gln1520=
ENST00000350026.9:c.4521G=	ENSP00000055163.7:p.Gln1507=
ENST00000414678.6:c.3087G=	ENSP00000412835.2:p.Gln1029=
NM_017519.2:c.4521G=	NP_059989.2:p.Gln1507=
NM_020732.3:c.4560G=	NP_065783.3:p.Gln1520=
XM_005267069.3:c.4680G=	XP_005267126.2:p.Gln1560=
XM_011535984.1:c.3759G=	XP_011534286.1:p.Gln1253=
XM_011535985.1:c.3579G=	XP_011534287.1:p.Gln1193=
XM_011535986.1:c.3339G=	XP_011534288.1:p.Gln1113=
XM_011535987.1:c.2958G=	XP_011534289.1:p.Gln986=
XM_011535988.1:c.1821G=	XP_011534290.1:p.Gln607=
NM_001346813.1:c.4680G=	NP_001333742.1:p.Gln1560=
NM_001363725.1:c.2430G=	NP_001350654.1:p.Gln810=
XM_011535984.2:c.4890G=	XP_011534286.2:p.Gln1630=
XM_011535988.3:c.1821G=	XP_011534290.1:p.Gln607=
XM_017011103.2:c.4791G=	XP_016866592.1:p.Gln1597=
XM_017011104.1:c.4761G=	XP_016866593.1:p.Gln1587=
XM_017011105.2:c.4731G=	XP_016866594.1:p.Gln1577=
XM_017011106.2:c.4602G=	XP_016866595.1:p.Gln1534=
XM_017011107.2:c.4581G=	XP_016866596.1:p.Gln1527=
XR_002956289.1:n.4876G=
NM_001363725.2:c.2430G=	NP_001350654.1:p.Gln810=
NM_001371656.1:c.4809G=	NP_001358585.1:p.Gln1603=
NM_001374820.1:c.4809G=	NP_001361749.1:p.Gln1603=
NM_001374828.1:c.4929G= MANE Select	NP_001361757.1:p.Gln1643=
NM_017519.3:c.4770G=	NP_059989.3:p.Gln1590=