Canonical Allele Identifier: CA366242044

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4736A>G	ENSP00000055163.8:p.Glu1579Gly
ENST00000414678.8:c.4805A>G	ENSP00000412835.3:p.Glu1602Gly
ENST00000637015.2:c.5024A>G	ENSP00000489729.2:p.Glu1675Gly
ENST00000346085.10:c.4775A>G	ENSP00000344546.5:p.Glu1592Gly
ENST00000350026.10:c.4487A>G	ENSP00000055163.7:p.Glu1496Gly
ENST00000414678.7:c.3053A>G	ENSP00000412835.2:p.Glu1018Gly
ENST00000635849.1:c.2216A>G	ENSP00000490948.1:p.Glu739Gly
ENST00000635957.1:c.1847A>G	ENSP00000490385.1:p.Glu616Gly
ENST00000636227.1:n.3358A>G
ENST00000636254.1:n.815A>G
ENST00000636930.2:c.4895A>G MANE Select	ENSP00000490491.2:p.Glu1632Gly
ENST00000636940.1:n.2892A>G
ENST00000637015.1:c.2263A>G
ENST00000637568.1:c.2177A>G
ENST00000637741.1:n.1561A>G
ENST00000637810.1:c.2237A>G	ENSP00000489636.1:p.Glu746Gly
ENST00000637904.1:c.2396A>G	ENSP00000490550.1:p.Glu799Gly
ENST00000647938.1:c.4526A>G	ENSP00000498155.1:p.Glu1509Gly
ENST00000346085.9:c.4526A>G	ENSP00000344546.4:p.Glu1509Gly
ENST00000350026.9:c.4487A>G	ENSP00000055163.7:p.Glu1496Gly
ENST00000414678.6:c.3053A>G	ENSP00000412835.2:p.Glu1018Gly
NM_017519.2:c.4487A>G	NP_059989.2:p.Glu1496Gly
NM_020732.3:c.4526A>G	NP_065783.3:p.Glu1509Gly
XM_005267069.3:c.4646A>G	XP_005267126.2:p.Glu1549Gly
XM_011535984.1:c.3725A>G	XP_011534286.1:p.Glu1242Gly
XM_011535985.1:c.3545A>G	XP_011534287.1:p.Glu1182Gly
XM_011535986.1:c.3305A>G	XP_011534288.1:p.Glu1102Gly
XM_011535987.1:c.2924A>G	XP_011534289.1:p.Glu975Gly
XM_011535988.1:c.1787A>G	XP_011534290.1:p.Glu596Gly
NM_001346813.1:c.4646A>G	NP_001333742.1:p.Glu1549Gly
NM_001363725.1:c.2396A>G	NP_001350654.1:p.Glu799Gly
XM_011535984.2:c.4856A>G	XP_011534286.2:p.Glu1619Gly
XM_011535988.3:c.1787A>G	XP_011534290.1:p.Glu596Gly
XM_017011103.2:c.4757A>G	XP_016866592.1:p.Glu1586Gly
XM_017011104.1:c.4727A>G	XP_016866593.1:p.Glu1576Gly
XM_017011105.2:c.4697A>G	XP_016866594.1:p.Glu1566Gly
XM_017011106.2:c.4568A>G	XP_016866595.1:p.Glu1523Gly
XM_017011107.2:c.4547A>G	XP_016866596.1:p.Glu1516Gly
XR_002956289.1:n.4842A>G
NM_001363725.2:c.2396A>G	NP_001350654.1:p.Glu799Gly
NM_001371656.1:c.4775A>G	NP_001358585.1:p.Glu1592Gly
NM_001374820.1:c.4775A>G	NP_001361749.1:p.Glu1592Gly
NM_001374828.1:c.4895A>G MANE Select	NP_001361757.1:p.Glu1632Gly
NM_017519.3:c.4736A>G	NP_059989.3:p.Glu1579Gly