Canonical Allele Identifier: CA1675523230

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201252C= , CM000668.2:g.157201252C=	GRCh38
NC_000006.11:g.157522386C= , CM000668.1:g.157522386C=	GRCh37
NC_000006.10:g.157564078C=	NCBI36
NG_032093.1:g.428323C=
NG_032093.2:g.428323C=
NG_066624.1:g.430227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4868C=	ENSP00000055163.8:p.Ala1623=
ENST00000414678.8:c.4937C=	ENSP00000412835.3:p.Ala1646=
ENST00000637015.2:c.5156C=	ENSP00000489729.2:p.Ala1719=
ENST00000346085.10:c.4907C=	ENSP00000344546.5:p.Ala1636=
ENST00000350026.10:c.4619C=	ENSP00000055163.7:p.Ala1540=
ENST00000414678.7:c.3185C=	ENSP00000412835.2:p.Ala1062=
ENST00000635849.1:c.2348C=	ENSP00000490948.1:p.Ala783=
ENST00000635957.1:c.1979C=	ENSP00000490385.1:p.Ala660=
ENST00000636227.1:n.3490C=
ENST00000636254.1:n.947C=
ENST00000636930.2:c.5027C= MANE Select	ENSP00000490491.2:p.Ala1676=
ENST00000636940.1:n.3024C=
ENST00000637015.1:c.2395C=
ENST00000637568.1:c.2309C=
ENST00000637741.1:n.1693C=
ENST00000637810.1:c.2369C=	ENSP00000489636.1:p.Ala790=
ENST00000637904.1:c.2528C=	ENSP00000490550.1:p.Ala843=
ENST00000647938.1:c.4658C=	ENSP00000498155.1:p.Ala1553=
ENST00000346085.9:c.4658C=	ENSP00000344546.4:p.Ala1553=
ENST00000350026.9:c.4619C=	ENSP00000055163.7:p.Ala1540=
ENST00000414678.6:c.3185C=	ENSP00000412835.2:p.Ala1062=
NM_017519.2:c.4619C=	NP_059989.2:p.Ala1540=
NM_020732.3:c.4658C=	NP_065783.3:p.Ala1553=
XM_005267069.3:c.4778C=	XP_005267126.2:p.Ala1593=
XM_011535984.1:c.3857C=	XP_011534286.1:p.Ala1286=
XM_011535985.1:c.3677C=	XP_011534287.1:p.Ala1226=
XM_011535986.1:c.3437C=	XP_011534288.1:p.Ala1146=
XM_011535987.1:c.3056C=	XP_011534289.1:p.Ala1019=
XM_011535988.1:c.1919C=	XP_011534290.1:p.Ala640=
NM_001346813.1:c.4778C=	NP_001333742.1:p.Ala1593=
NM_001363725.1:c.2528C=	NP_001350654.1:p.Ala843=
XM_011535984.2:c.4988C=	XP_011534286.2:p.Ala1663=
XM_011535988.3:c.1919C=	XP_011534290.1:p.Ala640=
XM_017011103.2:c.4889C=	XP_016866592.1:p.Ala1630=
XM_017011104.1:c.4859C=	XP_016866593.1:p.Ala1620=
XM_017011105.2:c.4829C=	XP_016866594.1:p.Ala1610=
XM_017011106.2:c.4700C=	XP_016866595.1:p.Ala1567=
XM_017011107.2:c.4679C=	XP_016866596.1:p.Ala1560=
XR_002956289.1:n.4974C=
NM_001363725.2:c.2528C=	NP_001350654.1:p.Ala843=
NM_001371656.1:c.4907C=	NP_001358585.1:p.Ala1636=
NM_001374820.1:c.4907C=	NP_001361749.1:p.Ala1636=
NM_001374828.1:c.5027C= MANE Select	NP_001361757.1:p.Ala1676=
NM_017519.3:c.4868C=	NP_059989.3:p.Ala1623=