Canonical Allele Identifier: CA4067730

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1211601
• ClinVar RCV Id: RCV001583410
• dbSNP Id: rs773006123
• ExAC: 6:157522255 G / A
• gnomAD v2: 6-157522255-G-A
• gnomAD v3: 6-157201121-G-A
• gnomAD v4: 6-157201121-G-A
• MyVariant Identifiers: chr6:g.157522255G>A (hg19) ; chr6:g.157201121G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201121G>A , CM000668.2:g.157201121G>A	GRCh38
NC_000006.11:g.157522255G>A , CM000668.1:g.157522255G>A	GRCh37
NC_000006.10:g.157563947G>A	NCBI36
NG_032093.1:g.428192G>A
NG_032093.2:g.428192G>A
NG_066624.1:g.430096G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4737G>A	ENSP00000055163.8:p.Glu1579=
ENST00000414678.8:c.4806G>A	ENSP00000412835.3:p.Glu1602=
ENST00000637015.2:c.5025G>A	ENSP00000489729.2:p.Glu1675=
ENST00000346085.10:c.4776G>A	ENSP00000344546.5:p.Glu1592=
ENST00000350026.10:c.4488G>A	ENSP00000055163.7:p.Glu1496=
ENST00000414678.7:c.3054G>A	ENSP00000412835.2:p.Glu1018=
ENST00000635849.1:c.2217G>A	ENSP00000490948.1:p.Glu739=
ENST00000635957.1:c.1848G>A	ENSP00000490385.1:p.Glu616=
ENST00000636227.1:n.3359G>A
ENST00000636254.1:n.816G>A
ENST00000636930.2:c.4896G>A MANE Select	ENSP00000490491.2:p.Glu1632=
ENST00000636940.1:n.2893G>A
ENST00000637015.1:c.2264G>A
ENST00000637568.1:c.2178G>A
ENST00000637741.1:n.1562G>A
ENST00000637810.1:c.2238G>A	ENSP00000489636.1:p.Glu746=
ENST00000637904.1:c.2397G>A	ENSP00000490550.1:p.Glu799=
ENST00000647938.1:c.4527G>A	ENSP00000498155.1:p.Glu1509=
ENST00000346085.9:c.4527G>A	ENSP00000344546.4:p.Glu1509=
ENST00000350026.9:c.4488G>A	ENSP00000055163.7:p.Glu1496=
ENST00000414678.6:c.3054G>A	ENSP00000412835.2:p.Glu1018=
NM_017519.2:c.4488G>A	NP_059989.2:p.Glu1496=
NM_020732.3:c.4527G>A	NP_065783.3:p.Glu1509=
XM_005267069.3:c.4647G>A	XP_005267126.2:p.Glu1549=
XM_011535984.1:c.3726G>A	XP_011534286.1:p.Glu1242=
XM_011535985.1:c.3546G>A	XP_011534287.1:p.Glu1182=
XM_011535986.1:c.3306G>A	XP_011534288.1:p.Glu1102=
XM_011535987.1:c.2925G>A	XP_011534289.1:p.Glu975=
XM_011535988.1:c.1788G>A	XP_011534290.1:p.Glu596=
NM_001346813.1:c.4647G>A	NP_001333742.1:p.Glu1549=
NM_001363725.1:c.2397G>A	NP_001350654.1:p.Glu799=
XM_011535984.2:c.4857G>A	XP_011534286.2:p.Glu1619=
XM_011535988.3:c.1788G>A	XP_011534290.1:p.Glu596=
XM_017011103.2:c.4758G>A	XP_016866592.1:p.Glu1586=
XM_017011104.1:c.4728G>A	XP_016866593.1:p.Glu1576=
XM_017011105.2:c.4698G>A	XP_016866594.1:p.Glu1566=
XM_017011106.2:c.4569G>A	XP_016866595.1:p.Glu1523=
XM_017011107.2:c.4548G>A	XP_016866596.1:p.Glu1516=
XR_002956289.1:n.4843G>A
NM_001363725.2:c.2397G>A	NP_001350654.1:p.Glu799=
NM_001371656.1:c.4776G>A	NP_001358585.1:p.Glu1592=
NM_001374820.1:c.4776G>A	NP_001361749.1:p.Glu1592=
NM_001374828.1:c.4896G>A MANE Select	NP_001361757.1:p.Glu1632=
NM_017519.3:c.4737G>A	NP_059989.3:p.Glu1579=