Canonical Allele Identifier: CA1675522826

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201032G= , CM000668.2:g.157201032G=	GRCh38
NC_000006.11:g.157522166G= , CM000668.1:g.157522166G=	GRCh37
NC_000006.10:g.157563858G=	NCBI36
NG_032093.1:g.428103G=
NG_032093.2:g.428103G=
NG_066624.1:g.430007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4648G=	ENSP00000055163.8:p.Gly1550=
ENST00000414678.8:c.4717G=	ENSP00000412835.3:p.Gly1573=
ENST00000637015.2:c.4936G=	ENSP00000489729.2:p.Gly1646=
ENST00000346085.10:c.4687G=	ENSP00000344546.5:p.Gly1563=
ENST00000350026.10:c.4399G=	ENSP00000055163.7:p.Gly1467=
ENST00000414678.7:c.2965G=	ENSP00000412835.2:p.Gly989=
ENST00000635849.1:c.2128G=	ENSP00000490948.1:p.Gly710=
ENST00000635957.1:c.1759G=	ENSP00000490385.1:p.Gly587=
ENST00000636227.1:n.3270G=
ENST00000636254.1:n.727G=
ENST00000636930.2:c.4807G= MANE Select	ENSP00000490491.2:p.Gly1603=
ENST00000636940.1:n.2804G=
ENST00000637015.1:c.2175G=
ENST00000637568.1:c.2089G=
ENST00000637741.1:n.1473G=
ENST00000637810.1:c.2149G=	ENSP00000489636.1:p.Gly717=
ENST00000637904.1:c.2308G=	ENSP00000490550.1:p.Gly770=
ENST00000647938.1:c.4438G=	ENSP00000498155.1:p.Gly1480=
ENST00000346085.9:c.4438G=	ENSP00000344546.4:p.Gly1480=
ENST00000350026.9:c.4399G=	ENSP00000055163.7:p.Gly1467=
ENST00000414678.6:c.2965G=	ENSP00000412835.2:p.Gly989=
NM_017519.2:c.4399G=	NP_059989.2:p.Gly1467=
NM_020732.3:c.4438G=	NP_065783.3:p.Gly1480=
XM_005267069.3:c.4558G=	XP_005267126.2:p.Gly1520=
XM_011535984.1:c.3637G=	XP_011534286.1:p.Gly1213=
XM_011535985.1:c.3457G=	XP_011534287.1:p.Gly1153=
XM_011535986.1:c.3217G=	XP_011534288.1:p.Gly1073=
XM_011535987.1:c.2836G=	XP_011534289.1:p.Gly946=
XM_011535988.1:c.1699G=	XP_011534290.1:p.Gly567=
NM_001346813.1:c.4558G=	NP_001333742.1:p.Gly1520=
NM_001363725.1:c.2308G=	NP_001350654.1:p.Gly770=
XM_011535984.2:c.4768G=	XP_011534286.2:p.Gly1590=
XM_011535988.3:c.1699G=	XP_011534290.1:p.Gly567=
XM_017011103.2:c.4669G=	XP_016866592.1:p.Gly1557=
XM_017011104.1:c.4639G=	XP_016866593.1:p.Gly1547=
XM_017011105.2:c.4609G=	XP_016866594.1:p.Gly1537=
XM_017011106.2:c.4480G=	XP_016866595.1:p.Gly1494=
XM_017011107.2:c.4459G=	XP_016866596.1:p.Gly1487=
XR_002956289.1:n.4754G=
NM_001363725.2:c.2308G=	NP_001350654.1:p.Gly770=
NM_001371656.1:c.4687G=	NP_001358585.1:p.Gly1563=
NM_001374820.1:c.4687G=	NP_001361749.1:p.Gly1563=
NM_001374828.1:c.4807G= MANE Select	NP_001361757.1:p.Gly1603=
NM_017519.3:c.4648G=	NP_059989.3:p.Gly1550=