Canonical Allele Identifier: CA452978361

Gene: ARID1B

Linked Data

• dbSNP Id: rs1465735949
• gnomAD v2: 6-157522471-G-A
• MyVariant Identifiers: chr6:g.157522471G>A (hg19) ; chr6:g.157201337G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201337G>A , CM000668.2:g.157201337G>A	GRCh38
NC_000006.11:g.157522471G>A , CM000668.1:g.157522471G>A	GRCh37
NC_000006.10:g.157564163G>A	NCBI36
NG_032093.1:g.428408G>A
NG_032093.2:g.428408G>A
NG_066624.1:g.430312G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4953G>A	ENSP00000055163.8:p.Gln1651=
ENST00000414678.8:c.5022G>A	ENSP00000412835.3:p.Gln1674=
ENST00000637015.2:c.5241G>A	ENSP00000489729.2:p.Gln1747=
ENST00000346085.10:c.4992G>A	ENSP00000344546.5:p.Gln1664=
ENST00000350026.10:c.4704G>A	ENSP00000055163.7:p.Gln1568=
ENST00000414678.7:c.3270G>A	ENSP00000412835.2:p.Gln1090=
ENST00000635849.1:c.2433G>A	ENSP00000490948.1:p.Gln811=
ENST00000635957.1:c.2064G>A	ENSP00000490385.1:p.Gln688=
ENST00000636227.1:n.3575G>A
ENST00000636254.1:n.1032G>A
ENST00000636930.2:c.5112G>A MANE Select	ENSP00000490491.2:p.Gln1704=
ENST00000636940.1:n.3109G>A
ENST00000637015.1:c.2480G>A
ENST00000637568.1:c.2394G>A
ENST00000637741.1:n.1778G>A
ENST00000637810.1:c.2454G>A	ENSP00000489636.1:p.Gln818=
ENST00000637904.1:c.2613G>A	ENSP00000490550.1:p.Gln871=
ENST00000647938.1:c.4743G>A	ENSP00000498155.1:p.Gln1581=
ENST00000346085.9:c.4743G>A	ENSP00000344546.4:p.Gln1581=
ENST00000350026.9:c.4704G>A	ENSP00000055163.7:p.Gln1568=
ENST00000414678.6:c.3270G>A	ENSP00000412835.2:p.Gln1090=
NM_017519.2:c.4704G>A	NP_059989.2:p.Gln1568=
NM_020732.3:c.4743G>A	NP_065783.3:p.Gln1581=
XM_005267069.3:c.4863G>A	XP_005267126.2:p.Gln1621=
XM_011535984.1:c.3942G>A	XP_011534286.1:p.Gln1314=
XM_011535985.1:c.3762G>A	XP_011534287.1:p.Gln1254=
XM_011535986.1:c.3522G>A	XP_011534288.1:p.Gln1174=
XM_011535987.1:c.3141G>A	XP_011534289.1:p.Gln1047=
XM_011535988.1:c.2004G>A	XP_011534290.1:p.Gln668=
NM_001346813.1:c.4863G>A	NP_001333742.1:p.Gln1621=
NM_001363725.1:c.2613G>A	NP_001350654.1:p.Gln871=
XM_011535984.2:c.5073G>A	XP_011534286.2:p.Gln1691=
XM_011535988.3:c.2004G>A	XP_011534290.1:p.Gln668=
XM_017011103.2:c.4974G>A	XP_016866592.1:p.Gln1658=
XM_017011104.1:c.4944G>A	XP_016866593.1:p.Gln1648=
XM_017011105.2:c.4914G>A	XP_016866594.1:p.Gln1638=
XM_017011106.2:c.4785G>A	XP_016866595.1:p.Gln1595=
XM_017011107.2:c.4764G>A	XP_016866596.1:p.Gln1588=
XR_002956289.1:n.5059G>A
NM_001363725.2:c.2613G>A	NP_001350654.1:p.Gln871=
NM_001371656.1:c.4992G>A	NP_001358585.1:p.Gln1664=
NM_001374820.1:c.4992G>A	NP_001361749.1:p.Gln1664=
NM_001374828.1:c.5112G>A MANE Select	NP_001361757.1:p.Gln1704=
NM_017519.3:c.4953G>A	NP_059989.3:p.Gln1651=