Canonical Allele Identifier: CA452978402

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374194
• gnomAD v4: 6-157201052-G-A
• MyVariant Identifiers: chr6:g.157522186G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201052G>A , CM000668.2:g.157201052G>A	GRCh38
NC_000006.11:g.157522186G>A , CM000668.1:g.157522186G>A	GRCh37
NC_000006.10:g.157563878G>A	NCBI36
NG_032093.1:g.428123G>A
NG_032093.2:g.428123G>A
NG_066624.1:g.430027G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4668G>A	ENSP00000055163.8:p.Gln1556=
ENST00000414678.8:c.4737G>A	ENSP00000412835.3:p.Gln1579=
ENST00000637015.2:c.4956G>A	ENSP00000489729.2:p.Gln1652=
ENST00000346085.10:c.4707G>A	ENSP00000344546.5:p.Gln1569=
ENST00000350026.10:c.4419G>A	ENSP00000055163.7:p.Gln1473=
ENST00000414678.7:c.2985G>A	ENSP00000412835.2:p.Gln995=
ENST00000635849.1:c.2148G>A	ENSP00000490948.1:p.Gln716=
ENST00000635957.1:c.1779G>A	ENSP00000490385.1:p.Gln593=
ENST00000636227.1:n.3290G>A
ENST00000636254.1:n.747G>A
ENST00000636930.2:c.4827G>A MANE Select	ENSP00000490491.2:p.Gln1609=
ENST00000636940.1:n.2824G>A
ENST00000637015.1:c.2195G>A
ENST00000637568.1:c.2109G>A
ENST00000637741.1:n.1493G>A
ENST00000637810.1:c.2169G>A	ENSP00000489636.1:p.Gln723=
ENST00000637904.1:c.2328G>A	ENSP00000490550.1:p.Gln776=
ENST00000647938.1:c.4458G>A	ENSP00000498155.1:p.Gln1486=
ENST00000346085.9:c.4458G>A	ENSP00000344546.4:p.Gln1486=
ENST00000350026.9:c.4419G>A	ENSP00000055163.7:p.Gln1473=
ENST00000414678.6:c.2985G>A	ENSP00000412835.2:p.Gln995=
NM_017519.2:c.4419G>A	NP_059989.2:p.Gln1473=
NM_020732.3:c.4458G>A	NP_065783.3:p.Gln1486=
XM_005267069.3:c.4578G>A	XP_005267126.2:p.Gln1526=
XM_011535984.1:c.3657G>A	XP_011534286.1:p.Gln1219=
XM_011535985.1:c.3477G>A	XP_011534287.1:p.Gln1159=
XM_011535986.1:c.3237G>A	XP_011534288.1:p.Gln1079=
XM_011535987.1:c.2856G>A	XP_011534289.1:p.Gln952=
XM_011535988.1:c.1719G>A	XP_011534290.1:p.Gln573=
NM_001346813.1:c.4578G>A	NP_001333742.1:p.Gln1526=
NM_001363725.1:c.2328G>A	NP_001350654.1:p.Gln776=
XM_011535984.2:c.4788G>A	XP_011534286.2:p.Gln1596=
XM_011535988.3:c.1719G>A	XP_011534290.1:p.Gln573=
XM_017011103.2:c.4689G>A	XP_016866592.1:p.Gln1563=
XM_017011104.1:c.4659G>A	XP_016866593.1:p.Gln1553=
XM_017011105.2:c.4629G>A	XP_016866594.1:p.Gln1543=
XM_017011106.2:c.4500G>A	XP_016866595.1:p.Gln1500=
XM_017011107.2:c.4479G>A	XP_016866596.1:p.Gln1493=
XR_002956289.1:n.4774G>A
NM_001363725.2:c.2328G>A	NP_001350654.1:p.Gln776=
NM_001371656.1:c.4707G>A	NP_001358585.1:p.Gln1569=
NM_001374820.1:c.4707G>A	NP_001361749.1:p.Gln1569=
NM_001374828.1:c.4827G>A MANE Select	NP_001361757.1:p.Gln1609=
NM_017519.3:c.4668G>A	NP_059989.3:p.Gln1556=