Canonical Allele Identifier: CA1675523276

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201267C= , CM000668.2:g.157201267C=	GRCh38
NC_000006.11:g.157522401C= , CM000668.1:g.157522401C=	GRCh37
NC_000006.10:g.157564093C=	NCBI36
NG_032093.1:g.428338C=
NG_032093.2:g.428338C=
NG_066624.1:g.430242C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4883C=	ENSP00000055163.8:p.Ser1628=
ENST00000414678.8:c.4952C=	ENSP00000412835.3:p.Ser1651=
ENST00000637015.2:c.5171C=	ENSP00000489729.2:p.Ser1724=
ENST00000346085.10:c.4922C=	ENSP00000344546.5:p.Ser1641=
ENST00000350026.10:c.4634C=	ENSP00000055163.7:p.Ser1545=
ENST00000414678.7:c.3200C=	ENSP00000412835.2:p.Ser1067=
ENST00000635849.1:c.2363C=	ENSP00000490948.1:p.Ser788=
ENST00000635957.1:c.1994C=	ENSP00000490385.1:p.Ser665=
ENST00000636227.1:n.3505C=
ENST00000636254.1:n.962C=
ENST00000636930.2:c.5042C= MANE Select	ENSP00000490491.2:p.Ser1681=
ENST00000636940.1:n.3039C=
ENST00000637015.1:c.2410C=
ENST00000637568.1:c.2324C=
ENST00000637741.1:n.1708C=
ENST00000637810.1:c.2384C=	ENSP00000489636.1:p.Ser795=
ENST00000637904.1:c.2543C=	ENSP00000490550.1:p.Ser848=
ENST00000647938.1:c.4673C=	ENSP00000498155.1:p.Ser1558=
ENST00000346085.9:c.4673C=	ENSP00000344546.4:p.Ser1558=
ENST00000350026.9:c.4634C=	ENSP00000055163.7:p.Ser1545=
ENST00000414678.6:c.3200C=	ENSP00000412835.2:p.Ser1067=
NM_017519.2:c.4634C=	NP_059989.2:p.Ser1545=
NM_020732.3:c.4673C=	NP_065783.3:p.Ser1558=
XM_005267069.3:c.4793C=	XP_005267126.2:p.Ser1598=
XM_011535984.1:c.3872C=	XP_011534286.1:p.Ser1291=
XM_011535985.1:c.3692C=	XP_011534287.1:p.Ser1231=
XM_011535986.1:c.3452C=	XP_011534288.1:p.Ser1151=
XM_011535987.1:c.3071C=	XP_011534289.1:p.Ser1024=
XM_011535988.1:c.1934C=	XP_011534290.1:p.Ser645=
NM_001346813.1:c.4793C=	NP_001333742.1:p.Ser1598=
NM_001363725.1:c.2543C=	NP_001350654.1:p.Ser848=
XM_011535984.2:c.5003C=	XP_011534286.2:p.Ser1668=
XM_011535988.3:c.1934C=	XP_011534290.1:p.Ser645=
XM_017011103.2:c.4904C=	XP_016866592.1:p.Ser1635=
XM_017011104.1:c.4874C=	XP_016866593.1:p.Ser1625=
XM_017011105.2:c.4844C=	XP_016866594.1:p.Ser1615=
XM_017011106.2:c.4715C=	XP_016866595.1:p.Ser1572=
XM_017011107.2:c.4694C=	XP_016866596.1:p.Ser1565=
XR_002956289.1:n.4989C=
NM_001363725.2:c.2543C=	NP_001350654.1:p.Ser848=
NM_001371656.1:c.4922C=	NP_001358585.1:p.Ser1641=
NM_001374820.1:c.4922C=	NP_001361749.1:p.Ser1641=
NM_001374828.1:c.5042C= MANE Select	NP_001361757.1:p.Ser1681=
NM_017519.3:c.4883C=	NP_059989.3:p.Ser1628=