Canonical Allele Identifier: CA150370387

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2172361
• ClinVar RCV Id: RCV003090540
• dbSNP Id: rs556299458
• gnomAD v2: 6-157522420-G-A
• gnomAD v4: 6-157201286-G-A
• MyVariant Identifiers: chr6:g.157522420G>A (hg19) ; chr6:g.157201286G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201286G>A , CM000668.2:g.157201286G>A	GRCh38
NC_000006.11:g.157522420G>A , CM000668.1:g.157522420G>A	GRCh37
NC_000006.10:g.157564112G>A	NCBI36
NG_032093.1:g.428357G>A
NG_032093.2:g.428357G>A
NG_066624.1:g.430261G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4902G>A	ENSP00000055163.8:p.Glu1634=
ENST00000414678.8:c.4971G>A	ENSP00000412835.3:p.Glu1657=
ENST00000637015.2:c.5190G>A	ENSP00000489729.2:p.Glu1730=
ENST00000346085.10:c.4941G>A	ENSP00000344546.5:p.Glu1647=
ENST00000350026.10:c.4653G>A	ENSP00000055163.7:p.Glu1551=
ENST00000414678.7:c.3219G>A	ENSP00000412835.2:p.Glu1073=
ENST00000635849.1:c.2382G>A	ENSP00000490948.1:p.Glu794=
ENST00000635957.1:c.2013G>A	ENSP00000490385.1:p.Glu671=
ENST00000636227.1:n.3524G>A
ENST00000636254.1:n.981G>A
ENST00000636930.2:c.5061G>A MANE Select	ENSP00000490491.2:p.Glu1687=
ENST00000636940.1:n.3058G>A
ENST00000637015.1:c.2429G>A
ENST00000637568.1:c.2343G>A
ENST00000637741.1:n.1727G>A
ENST00000637810.1:c.2403G>A	ENSP00000489636.1:p.Glu801=
ENST00000637904.1:c.2562G>A	ENSP00000490550.1:p.Glu854=
ENST00000647938.1:c.4692G>A	ENSP00000498155.1:p.Glu1564=
ENST00000346085.9:c.4692G>A	ENSP00000344546.4:p.Glu1564=
ENST00000350026.9:c.4653G>A	ENSP00000055163.7:p.Glu1551=
ENST00000414678.6:c.3219G>A	ENSP00000412835.2:p.Glu1073=
NM_017519.2:c.4653G>A	NP_059989.2:p.Glu1551=
NM_020732.3:c.4692G>A	NP_065783.3:p.Glu1564=
XM_005267069.3:c.4812G>A	XP_005267126.2:p.Glu1604=
XM_011535984.1:c.3891G>A	XP_011534286.1:p.Glu1297=
XM_011535985.1:c.3711G>A	XP_011534287.1:p.Glu1237=
XM_011535986.1:c.3471G>A	XP_011534288.1:p.Glu1157=
XM_011535987.1:c.3090G>A	XP_011534289.1:p.Glu1030=
XM_011535988.1:c.1953G>A	XP_011534290.1:p.Glu651=
NM_001346813.1:c.4812G>A	NP_001333742.1:p.Glu1604=
NM_001363725.1:c.2562G>A	NP_001350654.1:p.Glu854=
XM_011535984.2:c.5022G>A	XP_011534286.2:p.Glu1674=
XM_011535988.3:c.1953G>A	XP_011534290.1:p.Glu651=
XM_017011103.2:c.4923G>A	XP_016866592.1:p.Glu1641=
XM_017011104.1:c.4893G>A	XP_016866593.1:p.Glu1631=
XM_017011105.2:c.4863G>A	XP_016866594.1:p.Glu1621=
XM_017011106.2:c.4734G>A	XP_016866595.1:p.Glu1578=
XM_017011107.2:c.4713G>A	XP_016866596.1:p.Glu1571=
XR_002956289.1:n.5008G>A
NM_001363725.2:c.2562G>A	NP_001350654.1:p.Glu854=
NM_001371656.1:c.4941G>A	NP_001358585.1:p.Glu1647=
NM_001374820.1:c.4941G>A	NP_001361749.1:p.Glu1647=
NM_001374828.1:c.5061G>A MANE Select	NP_001361757.1:p.Glu1687=
NM_017519.3:c.4902G>A	NP_059989.3:p.Glu1634=