Canonical Allele Identifier: CA452978074

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794063133
• gnomAD v3: 6-157200968-G-A
• gnomAD v4: 6-157200968-G-A
• MyVariant Identifiers: chr6:g.157522102G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200968G>A , CM000668.2:g.157200968G>A	GRCh38
NC_000006.11:g.157522102G>A , CM000668.1:g.157522102G>A	GRCh37
NC_000006.10:g.157563794G>A	NCBI36
NG_032093.1:g.428039G>A
NG_032093.2:g.428039G>A
NG_066624.1:g.429943G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4584G>A	ENSP00000055163.8:p.Glu1528=
ENST00000414678.8:c.4653G>A	ENSP00000412835.3:p.Glu1551=
ENST00000637015.2:c.4872G>A	ENSP00000489729.2:p.Glu1624=
ENST00000346085.10:c.4623G>A	ENSP00000344546.5:p.Glu1541=
ENST00000350026.10:c.4335G>A	ENSP00000055163.7:p.Glu1445=
ENST00000414678.7:c.2901G>A	ENSP00000412835.2:p.Glu967=
ENST00000635849.1:c.2064G>A	ENSP00000490948.1:p.Glu688=
ENST00000635957.1:c.1695G>A	ENSP00000490385.1:p.Glu565=
ENST00000636227.1:n.3206G>A
ENST00000636254.1:n.663G>A
ENST00000636930.2:c.4743G>A MANE Select	ENSP00000490491.2:p.Glu1581=
ENST00000636940.1:n.2740G>A
ENST00000637015.1:c.2111G>A
ENST00000637568.1:c.2025G>A
ENST00000637741.1:n.1409G>A
ENST00000637810.1:c.2085G>A	ENSP00000489636.1:p.Glu695=
ENST00000637904.1:c.2244G>A	ENSP00000490550.1:p.Glu748=
ENST00000647938.1:c.4374G>A	ENSP00000498155.1:p.Glu1458=
ENST00000346085.9:c.4374G>A	ENSP00000344546.4:p.Glu1458=
ENST00000350026.9:c.4335G>A	ENSP00000055163.7:p.Glu1445=
ENST00000414678.6:c.2901G>A	ENSP00000412835.2:p.Glu967=
NM_017519.2:c.4335G>A	NP_059989.2:p.Glu1445=
NM_020732.3:c.4374G>A	NP_065783.3:p.Glu1458=
XM_005267069.3:c.4494G>A	XP_005267126.2:p.Glu1498=
XM_011535984.1:c.3573G>A	XP_011534286.1:p.Glu1191=
XM_011535985.1:c.3393G>A	XP_011534287.1:p.Glu1131=
XM_011535986.1:c.3153G>A	XP_011534288.1:p.Glu1051=
XM_011535987.1:c.2772G>A	XP_011534289.1:p.Glu924=
XM_011535988.1:c.1635G>A	XP_011534290.1:p.Glu545=
NM_001346813.1:c.4494G>A	NP_001333742.1:p.Glu1498=
NM_001363725.1:c.2244G>A	NP_001350654.1:p.Glu748=
XM_011535984.2:c.4704G>A	XP_011534286.2:p.Glu1568=
XM_011535988.3:c.1635G>A	XP_011534290.1:p.Glu545=
XM_017011103.2:c.4605G>A	XP_016866592.1:p.Glu1535=
XM_017011104.1:c.4575G>A	XP_016866593.1:p.Glu1525=
XM_017011105.2:c.4545G>A	XP_016866594.1:p.Glu1515=
XM_017011106.2:c.4416G>A	XP_016866595.1:p.Glu1472=
XM_017011107.2:c.4395G>A	XP_016866596.1:p.Glu1465=
XR_002956289.1:n.4690G>A
NM_001363725.2:c.2244G>A	NP_001350654.1:p.Glu748=
NM_001371656.1:c.4623G>A	NP_001358585.1:p.Glu1541=
NM_001374820.1:c.4623G>A	NP_001361749.1:p.Glu1541=
NM_001374828.1:c.4743G>A MANE Select	NP_001361757.1:p.Glu1581=
NM_017519.3:c.4584G>A	NP_059989.3:p.Glu1528=