Canonical Allele Identifier: CA4067711

Gene: ARID1B

Linked Data

• dbSNP Id: rs774335434
• ExAC: 6:157522156 G / A
• gnomAD v2: 6-157522156-G-A
• gnomAD v4: 6-157201022-G-A
• MyVariant Identifiers: chr6:g.157522156G>A (hg19) ; chr6:g.157201022G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201022G>A , CM000668.2:g.157201022G>A	GRCh38
NC_000006.11:g.157522156G>A , CM000668.1:g.157522156G>A	GRCh37
NC_000006.10:g.157563848G>A	NCBI36
NG_032093.1:g.428093G>A
NG_032093.2:g.428093G>A
NG_066624.1:g.429997G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4638G>A	ENSP00000055163.8:p.Gln1546=
ENST00000414678.8:c.4707G>A	ENSP00000412835.3:p.Gln1569=
ENST00000637015.2:c.4926G>A	ENSP00000489729.2:p.Gln1642=
ENST00000346085.10:c.4677G>A	ENSP00000344546.5:p.Gln1559=
ENST00000350026.10:c.4389G>A	ENSP00000055163.7:p.Gln1463=
ENST00000414678.7:c.2955G>A	ENSP00000412835.2:p.Gln985=
ENST00000635849.1:c.2118G>A	ENSP00000490948.1:p.Gln706=
ENST00000635957.1:c.1749G>A	ENSP00000490385.1:p.Gln583=
ENST00000636227.1:n.3260G>A
ENST00000636254.1:n.717G>A
ENST00000636930.2:c.4797G>A MANE Select	ENSP00000490491.2:p.Gln1599=
ENST00000636940.1:n.2794G>A
ENST00000637015.1:c.2165G>A
ENST00000637568.1:c.2079G>A
ENST00000637741.1:n.1463G>A
ENST00000637810.1:c.2139G>A	ENSP00000489636.1:p.Gln713=
ENST00000637904.1:c.2298G>A	ENSP00000490550.1:p.Gln766=
ENST00000647938.1:c.4428G>A	ENSP00000498155.1:p.Gln1476=
ENST00000346085.9:c.4428G>A	ENSP00000344546.4:p.Gln1476=
ENST00000350026.9:c.4389G>A	ENSP00000055163.7:p.Gln1463=
ENST00000414678.6:c.2955G>A	ENSP00000412835.2:p.Gln985=
NM_017519.2:c.4389G>A	NP_059989.2:p.Gln1463=
NM_020732.3:c.4428G>A	NP_065783.3:p.Gln1476=
XM_005267069.3:c.4548G>A	XP_005267126.2:p.Gln1516=
XM_011535984.1:c.3627G>A	XP_011534286.1:p.Gln1209=
XM_011535985.1:c.3447G>A	XP_011534287.1:p.Gln1149=
XM_011535986.1:c.3207G>A	XP_011534288.1:p.Gln1069=
XM_011535987.1:c.2826G>A	XP_011534289.1:p.Gln942=
XM_011535988.1:c.1689G>A	XP_011534290.1:p.Gln563=
NM_001346813.1:c.4548G>A	NP_001333742.1:p.Gln1516=
NM_001363725.1:c.2298G>A	NP_001350654.1:p.Gln766=
XM_011535984.2:c.4758G>A	XP_011534286.2:p.Gln1586=
XM_011535988.3:c.1689G>A	XP_011534290.1:p.Gln563=
XM_017011103.2:c.4659G>A	XP_016866592.1:p.Gln1553=
XM_017011104.1:c.4629G>A	XP_016866593.1:p.Gln1543=
XM_017011105.2:c.4599G>A	XP_016866594.1:p.Gln1533=
XM_017011106.2:c.4470G>A	XP_016866595.1:p.Gln1490=
XM_017011107.2:c.4449G>A	XP_016866596.1:p.Gln1483=
XR_002956289.1:n.4744G>A
NM_001363725.2:c.2298G>A	NP_001350654.1:p.Gln766=
NM_001371656.1:c.4677G>A	NP_001358585.1:p.Gln1559=
NM_001374820.1:c.4677G>A	NP_001361749.1:p.Gln1559=
NM_001374828.1:c.4797G>A MANE Select	NP_001361757.1:p.Gln1599=
NM_017519.3:c.4638G>A	NP_059989.3:p.Gln1546=