Canonical Allele Identifier: CA452978049

Gene: ARID1B

Linked Data

• dbSNP Id: rs1354792101
• gnomAD v2: 6-157522087-G-A
• gnomAD v4: 6-157200953-G-A
• MyVariant Identifiers: chr6:g.157522087G>A (hg19) ; chr6:g.157200953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200953G>A , CM000668.2:g.157200953G>A	GRCh38
NC_000006.11:g.157522087G>A , CM000668.1:g.157522087G>A	GRCh37
NC_000006.10:g.157563779G>A	NCBI36
NG_032093.1:g.428024G>A
NG_032093.2:g.428024G>A
NG_066624.1:g.429928G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4569G>A	ENSP00000055163.8:p.Gln1523=
ENST00000414678.8:c.4638G>A	ENSP00000412835.3:p.Gln1546=
ENST00000637015.2:c.4857G>A	ENSP00000489729.2:p.Gln1619=
ENST00000346085.10:c.4608G>A	ENSP00000344546.5:p.Gln1536=
ENST00000350026.10:c.4320G>A	ENSP00000055163.7:p.Gln1440=
ENST00000414678.7:c.2886G>A	ENSP00000412835.2:p.Gln962=
ENST00000635849.1:c.2049G>A	ENSP00000490948.1:p.Gln683=
ENST00000635957.1:c.1680G>A	ENSP00000490385.1:p.Gln560=
ENST00000636227.1:n.3191G>A
ENST00000636254.1:n.648G>A
ENST00000636930.2:c.4728G>A MANE Select	ENSP00000490491.2:p.Gln1576=
ENST00000636940.1:n.2725G>A
ENST00000637015.1:c.2096G>A
ENST00000637568.1:c.2010G>A
ENST00000637741.1:n.1394G>A
ENST00000637810.1:c.2070G>A	ENSP00000489636.1:p.Gln690=
ENST00000637904.1:c.2229G>A	ENSP00000490550.1:p.Gln743=
ENST00000647938.1:c.4359G>A	ENSP00000498155.1:p.Gln1453=
ENST00000346085.9:c.4359G>A	ENSP00000344546.4:p.Gln1453=
ENST00000350026.9:c.4320G>A	ENSP00000055163.7:p.Gln1440=
ENST00000414678.6:c.2886G>A	ENSP00000412835.2:p.Gln962=
NM_017519.2:c.4320G>A	NP_059989.2:p.Gln1440=
NM_020732.3:c.4359G>A	NP_065783.3:p.Gln1453=
XM_005267069.3:c.4479G>A	XP_005267126.2:p.Gln1493=
XM_011535984.1:c.3558G>A	XP_011534286.1:p.Gln1186=
XM_011535985.1:c.3378G>A	XP_011534287.1:p.Gln1126=
XM_011535986.1:c.3138G>A	XP_011534288.1:p.Gln1046=
XM_011535987.1:c.2757G>A	XP_011534289.1:p.Gln919=
XM_011535988.1:c.1620G>A	XP_011534290.1:p.Gln540=
NM_001346813.1:c.4479G>A	NP_001333742.1:p.Gln1493=
NM_001363725.1:c.2229G>A	NP_001350654.1:p.Gln743=
XM_011535984.2:c.4689G>A	XP_011534286.2:p.Gln1563=
XM_011535988.3:c.1620G>A	XP_011534290.1:p.Gln540=
XM_017011103.2:c.4590G>A	XP_016866592.1:p.Gln1530=
XM_017011104.1:c.4560G>A	XP_016866593.1:p.Gln1520=
XM_017011105.2:c.4530G>A	XP_016866594.1:p.Gln1510=
XM_017011106.2:c.4401G>A	XP_016866595.1:p.Gln1467=
XM_017011107.2:c.4380G>A	XP_016866596.1:p.Gln1460=
XR_002956289.1:n.4675G>A
NM_001363725.2:c.2229G>A	NP_001350654.1:p.Gln743=
NM_001371656.1:c.4608G>A	NP_001358585.1:p.Gln1536=
NM_001374820.1:c.4608G>A	NP_001361749.1:p.Gln1536=
NM_001374828.1:c.4728G>A MANE Select	NP_001361757.1:p.Gln1576=
NM_017519.3:c.4569G>A	NP_059989.3:p.Gln1523=