Canonical Allele Identifier: CA366242120

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235845
• MyVariant Identifiers: chr6:g.157522286C>G (hg19) ; chr6:g.157201152C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201152C>G , CM000668.2:g.157201152C>G	GRCh38
NC_000006.11:g.157522286C>G , CM000668.1:g.157522286C>G	GRCh37
NC_000006.10:g.157563978C>G	NCBI36
NG_032093.1:g.428223C>G
NG_032093.2:g.428223C>G
NG_066624.1:g.430127C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4768C>G	ENSP00000055163.8:p.Gln1590Glu
ENST00000414678.8:c.4837C>G	ENSP00000412835.3:p.Gln1613Glu
ENST00000637015.2:c.5056C>G	ENSP00000489729.2:p.Gln1686Glu
ENST00000346085.10:c.4807C>G	ENSP00000344546.5:p.Gln1603Glu
ENST00000350026.10:c.4519C>G	ENSP00000055163.7:p.Gln1507Glu
ENST00000414678.7:c.3085C>G	ENSP00000412835.2:p.Gln1029Glu
ENST00000635849.1:c.2248C>G	ENSP00000490948.1:p.Gln750Glu
ENST00000635957.1:c.1879C>G	ENSP00000490385.1:p.Gln627Glu
ENST00000636227.1:n.3390C>G
ENST00000636254.1:n.847C>G
ENST00000636930.2:c.4927C>G MANE Select	ENSP00000490491.2:p.Gln1643Glu
ENST00000636940.1:n.2924C>G
ENST00000637015.1:c.2295C>G
ENST00000637568.1:c.2209C>G
ENST00000637741.1:n.1593C>G
ENST00000637810.1:c.2269C>G	ENSP00000489636.1:p.Gln757Glu
ENST00000637904.1:c.2428C>G	ENSP00000490550.1:p.Gln810Glu
ENST00000647938.1:c.4558C>G	ENSP00000498155.1:p.Gln1520Glu
ENST00000346085.9:c.4558C>G	ENSP00000344546.4:p.Gln1520Glu
ENST00000350026.9:c.4519C>G	ENSP00000055163.7:p.Gln1507Glu
ENST00000414678.6:c.3085C>G	ENSP00000412835.2:p.Gln1029Glu
NM_017519.2:c.4519C>G	NP_059989.2:p.Gln1507Glu
NM_020732.3:c.4558C>G	NP_065783.3:p.Gln1520Glu
XM_005267069.3:c.4678C>G	XP_005267126.2:p.Gln1560Glu
XM_011535984.1:c.3757C>G	XP_011534286.1:p.Gln1253Glu
XM_011535985.1:c.3577C>G	XP_011534287.1:p.Gln1193Glu
XM_011535986.1:c.3337C>G	XP_011534288.1:p.Gln1113Glu
XM_011535987.1:c.2956C>G	XP_011534289.1:p.Gln986Glu
XM_011535988.1:c.1819C>G	XP_011534290.1:p.Gln607Glu
NM_001346813.1:c.4678C>G	NP_001333742.1:p.Gln1560Glu
NM_001363725.1:c.2428C>G	NP_001350654.1:p.Gln810Glu
XM_011535984.2:c.4888C>G	XP_011534286.2:p.Gln1630Glu
XM_011535988.3:c.1819C>G	XP_011534290.1:p.Gln607Glu
XM_017011103.2:c.4789C>G	XP_016866592.1:p.Gln1597Glu
XM_017011104.1:c.4759C>G	XP_016866593.1:p.Gln1587Glu
XM_017011105.2:c.4729C>G	XP_016866594.1:p.Gln1577Glu
XM_017011106.2:c.4600C>G	XP_016866595.1:p.Gln1534Glu
XM_017011107.2:c.4579C>G	XP_016866596.1:p.Gln1527Glu
XR_002956289.1:n.4874C>G
NM_001363725.2:c.2428C>G	NP_001350654.1:p.Gln810Glu
NM_001371656.1:c.4807C>G	NP_001358585.1:p.Gln1603Glu
NM_001374820.1:c.4807C>G	NP_001361749.1:p.Gln1603Glu
NM_001374828.1:c.4927C>G MANE Select	NP_001361757.1:p.Gln1643Glu
NM_017519.3:c.4768C>G	NP_059989.3:p.Gln1590Glu