Canonical Allele Identifier: CA1675523290

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201272C= , CM000668.2:g.157201272C=	GRCh38
NC_000006.11:g.157522406C= , CM000668.1:g.157522406C=	GRCh37
NC_000006.10:g.157564098C=	NCBI36
NG_032093.1:g.428343C=
NG_032093.2:g.428343C=
NG_066624.1:g.430247C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4888C=	ENSP00000055163.8:p.Gln1630=
ENST00000414678.8:c.4957C=	ENSP00000412835.3:p.Gln1653=
ENST00000637015.2:c.5176C=	ENSP00000489729.2:p.Gln1726=
ENST00000346085.10:c.4927C=	ENSP00000344546.5:p.Gln1643=
ENST00000350026.10:c.4639C=	ENSP00000055163.7:p.Gln1547=
ENST00000414678.7:c.3205C=	ENSP00000412835.2:p.Gln1069=
ENST00000635849.1:c.2368C=	ENSP00000490948.1:p.Gln790=
ENST00000635957.1:c.1999C=	ENSP00000490385.1:p.Gln667=
ENST00000636227.1:n.3510C=
ENST00000636254.1:n.967C=
ENST00000636930.2:c.5047C= MANE Select	ENSP00000490491.2:p.Gln1683=
ENST00000636940.1:n.3044C=
ENST00000637015.1:c.2415C=
ENST00000637568.1:c.2329C=
ENST00000637741.1:n.1713C=
ENST00000637810.1:c.2389C=	ENSP00000489636.1:p.Gln797=
ENST00000637904.1:c.2548C=	ENSP00000490550.1:p.Gln850=
ENST00000647938.1:c.4678C=	ENSP00000498155.1:p.Gln1560=
ENST00000346085.9:c.4678C=	ENSP00000344546.4:p.Gln1560=
ENST00000350026.9:c.4639C=	ENSP00000055163.7:p.Gln1547=
ENST00000414678.6:c.3205C=	ENSP00000412835.2:p.Gln1069=
NM_017519.2:c.4639C=	NP_059989.2:p.Gln1547=
NM_020732.3:c.4678C=	NP_065783.3:p.Gln1560=
XM_005267069.3:c.4798C=	XP_005267126.2:p.Gln1600=
XM_011535984.1:c.3877C=	XP_011534286.1:p.Gln1293=
XM_011535985.1:c.3697C=	XP_011534287.1:p.Gln1233=
XM_011535986.1:c.3457C=	XP_011534288.1:p.Gln1153=
XM_011535987.1:c.3076C=	XP_011534289.1:p.Gln1026=
XM_011535988.1:c.1939C=	XP_011534290.1:p.Gln647=
NM_001346813.1:c.4798C=	NP_001333742.1:p.Gln1600=
NM_001363725.1:c.2548C=	NP_001350654.1:p.Gln850=
XM_011535984.2:c.5008C=	XP_011534286.2:p.Gln1670=
XM_011535988.3:c.1939C=	XP_011534290.1:p.Gln647=
XM_017011103.2:c.4909C=	XP_016866592.1:p.Gln1637=
XM_017011104.1:c.4879C=	XP_016866593.1:p.Gln1627=
XM_017011105.2:c.4849C=	XP_016866594.1:p.Gln1617=
XM_017011106.2:c.4720C=	XP_016866595.1:p.Gln1574=
XM_017011107.2:c.4699C=	XP_016866596.1:p.Gln1567=
XR_002956289.1:n.4994C=
NM_001363725.2:c.2548C=	NP_001350654.1:p.Gln850=
NM_001371656.1:c.4927C=	NP_001358585.1:p.Gln1643=
NM_001374820.1:c.4927C=	NP_001361749.1:p.Gln1643=
NM_001374828.1:c.5047C= MANE Select	NP_001361757.1:p.Gln1683=
NM_017519.3:c.4888C=	NP_059989.3:p.Gln1630=