Canonical Allele Identifier: CA1675542221

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198830C= , CM000668.2:g.157198830C=	GRCh38
NC_000006.11:g.157519964C= , CM000668.1:g.157519964C=	GRCh37
NC_000006.10:g.157561656C=	NCBI36
NG_032093.1:g.425901C=
NG_032093.2:g.425901C=
NG_066624.1:g.427805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4243C=	ENSP00000055163.8:p.Gln1415=
ENST00000414678.8:c.4312C=	ENSP00000412835.3:p.Gln1438=
ENST00000637015.2:c.4531C=	ENSP00000489729.2:p.Gln1511=
ENST00000346085.10:c.4282C=	ENSP00000344546.5:p.Gln1428=
ENST00000350026.10:c.3994C=	ENSP00000055163.7:p.Gln1332=
ENST00000414678.7:c.2560C=	ENSP00000412835.2:p.Gln854=
ENST00000635849.1:c.1723C=	ENSP00000490948.1:p.Gln575=
ENST00000635957.1:c.1354C=	ENSP00000490385.1:p.Gln452=
ENST00000636227.1:n.2865C=
ENST00000636254.1:n.322C=
ENST00000636930.2:c.4402C= MANE Select	ENSP00000490491.2:p.Gln1468=
ENST00000636940.1:n.2399C=
ENST00000637015.1:c.1770C=
ENST00000637568.1:c.1684C=
ENST00000637741.1:n.1068C=
ENST00000637810.1:c.1744C=	ENSP00000489636.1:p.Gln582=
ENST00000637904.1:c.1903C=	ENSP00000490550.1:p.Gln635=
ENST00000647938.1:c.4033C=	ENSP00000498155.1:p.Gln1345=
ENST00000346085.9:c.4033C=	ENSP00000344546.4:p.Gln1345=
ENST00000350026.9:c.3994C=	ENSP00000055163.7:p.Gln1332=
ENST00000414678.6:c.2560C=	ENSP00000412835.2:p.Gln854=
NM_017519.2:c.3994C=	NP_059989.2:p.Gln1332=
NM_020732.3:c.4033C=	NP_065783.3:p.Gln1345=
XM_005267069.3:c.4153C=	XP_005267126.2:p.Gln1385=
XM_011535984.1:c.3232C=	XP_011534286.1:p.Gln1078=
XM_011535985.1:c.3052C=	XP_011534287.1:p.Gln1018=
XM_011535986.1:c.2812C=	XP_011534288.1:p.Gln938=
XM_011535987.1:c.2431C=	XP_011534289.1:p.Gln811=
XM_011535988.1:c.1294C=	XP_011534290.1:p.Gln432=
NM_001346813.1:c.4153C=	NP_001333742.1:p.Gln1385=
NM_001363725.1:c.1903C=	NP_001350654.1:p.Gln635=
XM_011535984.2:c.4363C=	XP_011534286.2:p.Gln1455=
XM_011535988.3:c.1294C=	XP_011534290.1:p.Gln432=
XM_017011103.2:c.4264C=	XP_016866592.1:p.Gln1422=
XM_017011104.1:c.4234C=	XP_016866593.1:p.Gln1412=
XM_017011105.2:c.4204C=	XP_016866594.1:p.Gln1402=
XM_017011106.2:c.4075C=	XP_016866595.1:p.Gln1359=
XM_017011107.2:c.4054C=	XP_016866596.1:p.Gln1352=
XR_002956289.1:n.4427-1875C=
NM_001363725.2:c.1903C=	NP_001350654.1:p.Gln635=
NM_001371656.1:c.4282C=	NP_001358585.1:p.Gln1428=
NM_001374820.1:c.4282C=	NP_001361749.1:p.Gln1428=
NM_001374828.1:c.4402C= MANE Select	NP_001361757.1:p.Gln1468=
NM_017519.3:c.4243C=	NP_059989.3:p.Gln1415=