Canonical Allele Identifier: CA4067700

Gene: ARID1B

Linked Data

• dbSNP Id: rs753891391
• ExAC: 6:157522111 G / A
• gnomAD v2: 6-157522111-G-A
• gnomAD v4: 6-157200977-G-A
• MyVariant Identifiers: chr6:g.157522111G>A (hg19) ; chr6:g.157200977G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200977G>A , CM000668.2:g.157200977G>A	GRCh38
NC_000006.11:g.157522111G>A , CM000668.1:g.157522111G>A	GRCh37
NC_000006.10:g.157563803G>A	NCBI36
NG_032093.1:g.428048G>A
NG_032093.2:g.428048G>A
NG_066624.1:g.429952G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4593G>A	ENSP00000055163.8:p.Gln1531=
ENST00000414678.8:c.4662G>A	ENSP00000412835.3:p.Gln1554=
ENST00000637015.2:c.4881G>A	ENSP00000489729.2:p.Gln1627=
ENST00000346085.10:c.4632G>A	ENSP00000344546.5:p.Gln1544=
ENST00000350026.10:c.4344G>A	ENSP00000055163.7:p.Gln1448=
ENST00000414678.7:c.2910G>A	ENSP00000412835.2:p.Gln970=
ENST00000635849.1:c.2073G>A	ENSP00000490948.1:p.Gln691=
ENST00000635957.1:c.1704G>A	ENSP00000490385.1:p.Gln568=
ENST00000636227.1:n.3215G>A
ENST00000636254.1:n.672G>A
ENST00000636930.2:c.4752G>A MANE Select	ENSP00000490491.2:p.Gln1584=
ENST00000636940.1:n.2749G>A
ENST00000637015.1:c.2120G>A
ENST00000637568.1:c.2034G>A
ENST00000637741.1:n.1418G>A
ENST00000637810.1:c.2094G>A	ENSP00000489636.1:p.Gln698=
ENST00000637904.1:c.2253G>A	ENSP00000490550.1:p.Gln751=
ENST00000647938.1:c.4383G>A	ENSP00000498155.1:p.Gln1461=
ENST00000346085.9:c.4383G>A	ENSP00000344546.4:p.Gln1461=
ENST00000350026.9:c.4344G>A	ENSP00000055163.7:p.Gln1448=
ENST00000414678.6:c.2910G>A	ENSP00000412835.2:p.Gln970=
NM_017519.2:c.4344G>A	NP_059989.2:p.Gln1448=
NM_020732.3:c.4383G>A	NP_065783.3:p.Gln1461=
XM_005267069.3:c.4503G>A	XP_005267126.2:p.Gln1501=
XM_011535984.1:c.3582G>A	XP_011534286.1:p.Gln1194=
XM_011535985.1:c.3402G>A	XP_011534287.1:p.Gln1134=
XM_011535986.1:c.3162G>A	XP_011534288.1:p.Gln1054=
XM_011535987.1:c.2781G>A	XP_011534289.1:p.Gln927=
XM_011535988.1:c.1644G>A	XP_011534290.1:p.Gln548=
NM_001346813.1:c.4503G>A	NP_001333742.1:p.Gln1501=
NM_001363725.1:c.2253G>A	NP_001350654.1:p.Gln751=
XM_011535984.2:c.4713G>A	XP_011534286.2:p.Gln1571=
XM_011535988.3:c.1644G>A	XP_011534290.1:p.Gln548=
XM_017011103.2:c.4614G>A	XP_016866592.1:p.Gln1538=
XM_017011104.1:c.4584G>A	XP_016866593.1:p.Gln1528=
XM_017011105.2:c.4554G>A	XP_016866594.1:p.Gln1518=
XM_017011106.2:c.4425G>A	XP_016866595.1:p.Gln1475=
XM_017011107.2:c.4404G>A	XP_016866596.1:p.Gln1468=
XR_002956289.1:n.4699G>A
NM_001363725.2:c.2253G>A	NP_001350654.1:p.Gln751=
NM_001371656.1:c.4632G>A	NP_001358585.1:p.Gln1544=
NM_001374820.1:c.4632G>A	NP_001361749.1:p.Gln1544=
NM_001374828.1:c.4752G>A MANE Select	NP_001361757.1:p.Gln1584=
NM_017519.3:c.4593G>A	NP_059989.3:p.Gln1531=