Canonical Allele Identifier: CA1675523033

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201130G= , CM000668.2:g.157201130G=	GRCh38
NC_000006.11:g.157522264G= , CM000668.1:g.157522264G=	GRCh37
NC_000006.10:g.157563956G=	NCBI36
NG_032093.1:g.428201G=
NG_032093.2:g.428201G=
NG_066624.1:g.430105G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4746G=	ENSP00000055163.8:p.Trp1582=
ENST00000414678.8:c.4815G=	ENSP00000412835.3:p.Trp1605=
ENST00000637015.2:c.5034G=	ENSP00000489729.2:p.Trp1678=
ENST00000346085.10:c.4785G=	ENSP00000344546.5:p.Trp1595=
ENST00000350026.10:c.4497G=	ENSP00000055163.7:p.Trp1499=
ENST00000414678.7:c.3063G=	ENSP00000412835.2:p.Trp1021=
ENST00000635849.1:c.2226G=	ENSP00000490948.1:p.Trp742=
ENST00000635957.1:c.1857G=	ENSP00000490385.1:p.Trp619=
ENST00000636227.1:n.3368G=
ENST00000636254.1:n.825G=
ENST00000636930.2:c.4905G= MANE Select	ENSP00000490491.2:p.Trp1635=
ENST00000636940.1:n.2902G=
ENST00000637015.1:c.2273G=
ENST00000637568.1:c.2187G=
ENST00000637741.1:n.1571G=
ENST00000637810.1:c.2247G=	ENSP00000489636.1:p.Trp749=
ENST00000637904.1:c.2406G=	ENSP00000490550.1:p.Trp802=
ENST00000647938.1:c.4536G=	ENSP00000498155.1:p.Trp1512=
ENST00000346085.9:c.4536G=	ENSP00000344546.4:p.Trp1512=
ENST00000350026.9:c.4497G=	ENSP00000055163.7:p.Trp1499=
ENST00000414678.6:c.3063G=	ENSP00000412835.2:p.Trp1021=
NM_017519.2:c.4497G=	NP_059989.2:p.Trp1499=
NM_020732.3:c.4536G=	NP_065783.3:p.Trp1512=
XM_005267069.3:c.4656G=	XP_005267126.2:p.Trp1552=
XM_011535984.1:c.3735G=	XP_011534286.1:p.Trp1245=
XM_011535985.1:c.3555G=	XP_011534287.1:p.Trp1185=
XM_011535986.1:c.3315G=	XP_011534288.1:p.Trp1105=
XM_011535987.1:c.2934G=	XP_011534289.1:p.Trp978=
XM_011535988.1:c.1797G=	XP_011534290.1:p.Trp599=
NM_001346813.1:c.4656G=	NP_001333742.1:p.Trp1552=
NM_001363725.1:c.2406G=	NP_001350654.1:p.Trp802=
XM_011535984.2:c.4866G=	XP_011534286.2:p.Trp1622=
XM_011535988.3:c.1797G=	XP_011534290.1:p.Trp599=
XM_017011103.2:c.4767G=	XP_016866592.1:p.Trp1589=
XM_017011104.1:c.4737G=	XP_016866593.1:p.Trp1579=
XM_017011105.2:c.4707G=	XP_016866594.1:p.Trp1569=
XM_017011106.2:c.4578G=	XP_016866595.1:p.Trp1526=
XM_017011107.2:c.4557G=	XP_016866596.1:p.Trp1519=
XR_002956289.1:n.4852G=
NM_001363725.2:c.2406G=	NP_001350654.1:p.Trp802=
NM_001371656.1:c.4785G=	NP_001358585.1:p.Trp1595=
NM_001374820.1:c.4785G=	NP_001361749.1:p.Trp1595=
NM_001374828.1:c.4905G= MANE Select	NP_001361757.1:p.Trp1635=
NM_017519.3:c.4746G=	NP_059989.3:p.Trp1582=