Canonical Allele Identifier: CA366242045

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522254A>T (hg19) ; chr6:g.157201120A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201120A>T , CM000668.2:g.157201120A>T	GRCh38
NC_000006.11:g.157522254A>T , CM000668.1:g.157522254A>T	GRCh37
NC_000006.10:g.157563946A>T	NCBI36
NG_032093.1:g.428191A>T
NG_032093.2:g.428191A>T
NG_066624.1:g.430095A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4736A>T	ENSP00000055163.8:p.Glu1579Val
ENST00000414678.8:c.4805A>T	ENSP00000412835.3:p.Glu1602Val
ENST00000637015.2:c.5024A>T	ENSP00000489729.2:p.Glu1675Val
ENST00000346085.10:c.4775A>T	ENSP00000344546.5:p.Glu1592Val
ENST00000350026.10:c.4487A>T	ENSP00000055163.7:p.Glu1496Val
ENST00000414678.7:c.3053A>T	ENSP00000412835.2:p.Glu1018Val
ENST00000635849.1:c.2216A>T	ENSP00000490948.1:p.Glu739Val
ENST00000635957.1:c.1847A>T	ENSP00000490385.1:p.Glu616Val
ENST00000636227.1:n.3358A>T
ENST00000636254.1:n.815A>T
ENST00000636930.2:c.4895A>T MANE Select	ENSP00000490491.2:p.Glu1632Val
ENST00000636940.1:n.2892A>T
ENST00000637015.1:c.2263A>T
ENST00000637568.1:c.2177A>T
ENST00000637741.1:n.1561A>T
ENST00000637810.1:c.2237A>T	ENSP00000489636.1:p.Glu746Val
ENST00000637904.1:c.2396A>T	ENSP00000490550.1:p.Glu799Val
ENST00000647938.1:c.4526A>T	ENSP00000498155.1:p.Glu1509Val
ENST00000346085.9:c.4526A>T	ENSP00000344546.4:p.Glu1509Val
ENST00000350026.9:c.4487A>T	ENSP00000055163.7:p.Glu1496Val
ENST00000414678.6:c.3053A>T	ENSP00000412835.2:p.Glu1018Val
NM_017519.2:c.4487A>T	NP_059989.2:p.Glu1496Val
NM_020732.3:c.4526A>T	NP_065783.3:p.Glu1509Val
XM_005267069.3:c.4646A>T	XP_005267126.2:p.Glu1549Val
XM_011535984.1:c.3725A>T	XP_011534286.1:p.Glu1242Val
XM_011535985.1:c.3545A>T	XP_011534287.1:p.Glu1182Val
XM_011535986.1:c.3305A>T	XP_011534288.1:p.Glu1102Val
XM_011535987.1:c.2924A>T	XP_011534289.1:p.Glu975Val
XM_011535988.1:c.1787A>T	XP_011534290.1:p.Glu596Val
NM_001346813.1:c.4646A>T	NP_001333742.1:p.Glu1549Val
NM_001363725.1:c.2396A>T	NP_001350654.1:p.Glu799Val
XM_011535984.2:c.4856A>T	XP_011534286.2:p.Glu1619Val
XM_011535988.3:c.1787A>T	XP_011534290.1:p.Glu596Val
XM_017011103.2:c.4757A>T	XP_016866592.1:p.Glu1586Val
XM_017011104.1:c.4727A>T	XP_016866593.1:p.Glu1576Val
XM_017011105.2:c.4697A>T	XP_016866594.1:p.Glu1566Val
XM_017011106.2:c.4568A>T	XP_016866595.1:p.Glu1523Val
XM_017011107.2:c.4547A>T	XP_016866596.1:p.Glu1516Val
XR_002956289.1:n.4842A>T
NM_001363725.2:c.2396A>T	NP_001350654.1:p.Glu799Val
NM_001371656.1:c.4775A>T	NP_001358585.1:p.Glu1592Val
NM_001374820.1:c.4775A>T	NP_001361749.1:p.Glu1592Val
NM_001374828.1:c.4895A>T MANE Select	NP_001361757.1:p.Glu1632Val
NM_017519.3:c.4736A>T	NP_059989.3:p.Glu1579Val