Canonical Allele Identifier: CA1675523029

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201127G= , CM000668.2:g.157201127G=	GRCh38
NC_000006.11:g.157522261G= , CM000668.1:g.157522261G=	GRCh37
NC_000006.10:g.157563953G=	NCBI36
NG_032093.1:g.428198G=
NG_032093.2:g.428198G=
NG_066624.1:g.430102G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4743G=	ENSP00000055163.8:p.Gln1581=
ENST00000414678.8:c.4812G=	ENSP00000412835.3:p.Gln1604=
ENST00000637015.2:c.5031G=	ENSP00000489729.2:p.Gln1677=
ENST00000346085.10:c.4782G=	ENSP00000344546.5:p.Gln1594=
ENST00000350026.10:c.4494G=	ENSP00000055163.7:p.Gln1498=
ENST00000414678.7:c.3060G=	ENSP00000412835.2:p.Gln1020=
ENST00000635849.1:c.2223G=	ENSP00000490948.1:p.Gln741=
ENST00000635957.1:c.1854G=	ENSP00000490385.1:p.Gln618=
ENST00000636227.1:n.3365G=
ENST00000636254.1:n.822G=
ENST00000636930.2:c.4902G= MANE Select	ENSP00000490491.2:p.Gln1634=
ENST00000636940.1:n.2899G=
ENST00000637015.1:c.2270G=
ENST00000637568.1:c.2184G=
ENST00000637741.1:n.1568G=
ENST00000637810.1:c.2244G=	ENSP00000489636.1:p.Gln748=
ENST00000637904.1:c.2403G=	ENSP00000490550.1:p.Gln801=
ENST00000647938.1:c.4533G=	ENSP00000498155.1:p.Gln1511=
ENST00000346085.9:c.4533G=	ENSP00000344546.4:p.Gln1511=
ENST00000350026.9:c.4494G=	ENSP00000055163.7:p.Gln1498=
ENST00000414678.6:c.3060G=	ENSP00000412835.2:p.Gln1020=
NM_017519.2:c.4494G=	NP_059989.2:p.Gln1498=
NM_020732.3:c.4533G=	NP_065783.3:p.Gln1511=
XM_005267069.3:c.4653G=	XP_005267126.2:p.Gln1551=
XM_011535984.1:c.3732G=	XP_011534286.1:p.Gln1244=
XM_011535985.1:c.3552G=	XP_011534287.1:p.Gln1184=
XM_011535986.1:c.3312G=	XP_011534288.1:p.Gln1104=
XM_011535987.1:c.2931G=	XP_011534289.1:p.Gln977=
XM_011535988.1:c.1794G=	XP_011534290.1:p.Gln598=
NM_001346813.1:c.4653G=	NP_001333742.1:p.Gln1551=
NM_001363725.1:c.2403G=	NP_001350654.1:p.Gln801=
XM_011535984.2:c.4863G=	XP_011534286.2:p.Gln1621=
XM_011535988.3:c.1794G=	XP_011534290.1:p.Gln598=
XM_017011103.2:c.4764G=	XP_016866592.1:p.Gln1588=
XM_017011104.1:c.4734G=	XP_016866593.1:p.Gln1578=
XM_017011105.2:c.4704G=	XP_016866594.1:p.Gln1568=
XM_017011106.2:c.4575G=	XP_016866595.1:p.Gln1525=
XM_017011107.2:c.4554G=	XP_016866596.1:p.Gln1518=
XR_002956289.1:n.4849G=
NM_001363725.2:c.2403G=	NP_001350654.1:p.Gln801=
NM_001371656.1:c.4782G=	NP_001358585.1:p.Gln1594=
NM_001374820.1:c.4782G=	NP_001361749.1:p.Gln1594=
NM_001374828.1:c.4902G= MANE Select	NP_001361757.1:p.Gln1634=
NM_017519.3:c.4743G=	NP_059989.3:p.Gln1581=