Canonical Allele Identifier: CA1675541085

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196221C= , CM000668.2:g.157196221C=	GRCh38
NC_000006.11:g.157517355C= , CM000668.1:g.157517355C=	GRCh37
NC_000006.10:g.157559047C=	NCBI36
NG_032093.1:g.423292C=
NG_032093.2:g.423292C=
NG_066624.1:g.425196C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4129C=	ENSP00000055163.8:p.Gln1377=
ENST00000414678.8:c.4198C=	ENSP00000412835.3:p.Gln1400=
ENST00000637015.2:c.4417C=	ENSP00000489729.2:p.Gln1473=
ENST00000346085.10:c.4168C=	ENSP00000344546.5:p.Gln1390=
ENST00000350026.10:c.3880C=	ENSP00000055163.7:p.Gln1294=
ENST00000414678.7:c.2446C=	ENSP00000412835.2:p.Gln816=
ENST00000635849.1:c.1609C=	ENSP00000490948.1:p.Gln537=
ENST00000635957.1:c.1240C=	ENSP00000490385.1:p.Gln414=
ENST00000636227.1:n.2751C=
ENST00000636930.2:c.4288C= MANE Select	ENSP00000490491.2:p.Gln1430=
ENST00000636940.1:n.2285C=
ENST00000637015.1:c.1656C=
ENST00000637568.1:c.1570C=
ENST00000637741.1:n.954C=
ENST00000637810.1:c.1630C=	ENSP00000489636.1:p.Gln544=
ENST00000637904.1:c.1789C=	ENSP00000490550.1:p.Gln597=
ENST00000647938.1:c.3919C=	ENSP00000498155.1:p.Gln1307=
ENST00000346085.9:c.3919C=	ENSP00000344546.4:p.Gln1307=
ENST00000350026.9:c.3880C=	ENSP00000055163.7:p.Gln1294=
ENST00000414678.6:c.2446C=	ENSP00000412835.2:p.Gln816=
NM_017519.2:c.3880C=	NP_059989.2:p.Gln1294=
NM_020732.3:c.3919C=	NP_065783.3:p.Gln1307=
XM_005267069.3:c.4039C=	XP_005267126.2:p.Gln1347=
XM_011535984.1:c.3118C=	XP_011534286.1:p.Gln1040=
XM_011535985.1:c.2938C=	XP_011534287.1:p.Gln980=
XM_011535986.1:c.2698C=	XP_011534288.1:p.Gln900=
XM_011535987.1:c.2317C=	XP_011534289.1:p.Gln773=
XM_011535988.1:c.1180C=	XP_011534290.1:p.Gln394=
NM_001346813.1:c.4039C=	NP_001333742.1:p.Gln1347=
NM_001363725.1:c.1789C=	NP_001350654.1:p.Gln597=
XM_011535984.2:c.4249C=	XP_011534286.2:p.Gln1417=
XM_011535988.3:c.1180C=	XP_011534290.1:p.Gln394=
XM_017011103.2:c.4150C=	XP_016866592.1:p.Gln1384=
XM_017011104.1:c.4120C=	XP_016866593.1:p.Gln1374=
XM_017011105.2:c.4090C=	XP_016866594.1:p.Gln1364=
XM_017011106.2:c.3961C=	XP_016866595.1:p.Gln1321=
XM_017011107.2:c.3940C=	XP_016866596.1:p.Gln1314=
XR_002956289.1:n.4332C=
NM_001363725.2:c.1789C=	NP_001350654.1:p.Gln597=
NM_001371656.1:c.4168C=	NP_001358585.1:p.Gln1390=
NM_001374820.1:c.4168C=	NP_001361749.1:p.Gln1390=
NM_001374828.1:c.4288C= MANE Select	NP_001361757.1:p.Gln1430=
NM_017519.3:c.4129C=	NP_059989.3:p.Gln1377=