Canonical Allele Identifier: CA1675523388

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201321C= , CM000668.2:g.157201321C=	GRCh38
NC_000006.11:g.157522455C= , CM000668.1:g.157522455C=	GRCh37
NC_000006.10:g.157564147C=	NCBI36
NG_032093.1:g.428392C=
NG_032093.2:g.428392C=
NG_066624.1:g.430296C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4937C=	ENSP00000055163.8:p.Pro1646=
ENST00000414678.8:c.5006C=	ENSP00000412835.3:p.Pro1669=
ENST00000637015.2:c.5225C=	ENSP00000489729.2:p.Pro1742=
ENST00000346085.10:c.4976C=	ENSP00000344546.5:p.Pro1659=
ENST00000350026.10:c.4688C=	ENSP00000055163.7:p.Pro1563=
ENST00000414678.7:c.3254C=	ENSP00000412835.2:p.Pro1085=
ENST00000635849.1:c.2417C=	ENSP00000490948.1:p.Pro806=
ENST00000635957.1:c.2048C=	ENSP00000490385.1:p.Pro683=
ENST00000636227.1:n.3559C=
ENST00000636254.1:n.1016C=
ENST00000636930.2:c.5096C= MANE Select	ENSP00000490491.2:p.Pro1699=
ENST00000636940.1:n.3093C=
ENST00000637015.1:c.2464C=
ENST00000637568.1:c.2378C=
ENST00000637741.1:n.1762C=
ENST00000637810.1:c.2438C=	ENSP00000489636.1:p.Pro813=
ENST00000637904.1:c.2597C=	ENSP00000490550.1:p.Pro866=
ENST00000647938.1:c.4727C=	ENSP00000498155.1:p.Pro1576=
ENST00000346085.9:c.4727C=	ENSP00000344546.4:p.Pro1576=
ENST00000350026.9:c.4688C=	ENSP00000055163.7:p.Pro1563=
ENST00000414678.6:c.3254C=	ENSP00000412835.2:p.Pro1085=
NM_017519.2:c.4688C=	NP_059989.2:p.Pro1563=
NM_020732.3:c.4727C=	NP_065783.3:p.Pro1576=
XM_005267069.3:c.4847C=	XP_005267126.2:p.Pro1616=
XM_011535984.1:c.3926C=	XP_011534286.1:p.Pro1309=
XM_011535985.1:c.3746C=	XP_011534287.1:p.Pro1249=
XM_011535986.1:c.3506C=	XP_011534288.1:p.Pro1169=
XM_011535987.1:c.3125C=	XP_011534289.1:p.Pro1042=
XM_011535988.1:c.1988C=	XP_011534290.1:p.Pro663=
NM_001346813.1:c.4847C=	NP_001333742.1:p.Pro1616=
NM_001363725.1:c.2597C=	NP_001350654.1:p.Pro866=
XM_011535984.2:c.5057C=	XP_011534286.2:p.Pro1686=
XM_011535988.3:c.1988C=	XP_011534290.1:p.Pro663=
XM_017011103.2:c.4958C=	XP_016866592.1:p.Pro1653=
XM_017011104.1:c.4928C=	XP_016866593.1:p.Pro1643=
XM_017011105.2:c.4898C=	XP_016866594.1:p.Pro1633=
XM_017011106.2:c.4769C=	XP_016866595.1:p.Pro1590=
XM_017011107.2:c.4748C=	XP_016866596.1:p.Pro1583=
XR_002956289.1:n.5043C=
NM_001363725.2:c.2597C=	NP_001350654.1:p.Pro866=
NM_001371656.1:c.4976C=	NP_001358585.1:p.Pro1659=
NM_001374820.1:c.4976C=	NP_001361749.1:p.Pro1659=
NM_001374828.1:c.5096C= MANE Select	NP_001361757.1:p.Pro1699=
NM_017519.3:c.4937C=	NP_059989.3:p.Pro1646=