Canonical Allele Identifier: CA366242059

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1506650
• ClinVar RCV Id: RCV002038153
• dbSNP Id: rs1794078806
• MyVariant Identifiers: chr6:g.157522260A>G (hg19) ; chr6:g.157201126A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201126A>G , CM000668.2:g.157201126A>G	GRCh38
NC_000006.11:g.157522260A>G , CM000668.1:g.157522260A>G	GRCh37
NC_000006.10:g.157563952A>G	NCBI36
NG_032093.1:g.428197A>G
NG_032093.2:g.428197A>G
NG_066624.1:g.430101A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4742A>G	ENSP00000055163.8:p.Gln1581Arg
ENST00000414678.8:c.4811A>G	ENSP00000412835.3:p.Gln1604Arg
ENST00000637015.2:c.5030A>G	ENSP00000489729.2:p.Gln1677Arg
ENST00000346085.10:c.4781A>G	ENSP00000344546.5:p.Gln1594Arg
ENST00000350026.10:c.4493A>G	ENSP00000055163.7:p.Gln1498Arg
ENST00000414678.7:c.3059A>G	ENSP00000412835.2:p.Gln1020Arg
ENST00000635849.1:c.2222A>G	ENSP00000490948.1:p.Gln741Arg
ENST00000635957.1:c.1853A>G	ENSP00000490385.1:p.Gln618Arg
ENST00000636227.1:n.3364A>G
ENST00000636254.1:n.821A>G
ENST00000636930.2:c.4901A>G MANE Select	ENSP00000490491.2:p.Gln1634Arg
ENST00000636940.1:n.2898A>G
ENST00000637015.1:c.2269A>G
ENST00000637568.1:c.2183A>G
ENST00000637741.1:n.1567A>G
ENST00000637810.1:c.2243A>G	ENSP00000489636.1:p.Gln748Arg
ENST00000637904.1:c.2402A>G	ENSP00000490550.1:p.Gln801Arg
ENST00000647938.1:c.4532A>G	ENSP00000498155.1:p.Gln1511Arg
ENST00000346085.9:c.4532A>G	ENSP00000344546.4:p.Gln1511Arg
ENST00000350026.9:c.4493A>G	ENSP00000055163.7:p.Gln1498Arg
ENST00000414678.6:c.3059A>G	ENSP00000412835.2:p.Gln1020Arg
NM_017519.2:c.4493A>G	NP_059989.2:p.Gln1498Arg
NM_020732.3:c.4532A>G	NP_065783.3:p.Gln1511Arg
XM_005267069.3:c.4652A>G	XP_005267126.2:p.Gln1551Arg
XM_011535984.1:c.3731A>G	XP_011534286.1:p.Gln1244Arg
XM_011535985.1:c.3551A>G	XP_011534287.1:p.Gln1184Arg
XM_011535986.1:c.3311A>G	XP_011534288.1:p.Gln1104Arg
XM_011535987.1:c.2930A>G	XP_011534289.1:p.Gln977Arg
XM_011535988.1:c.1793A>G	XP_011534290.1:p.Gln598Arg
NM_001346813.1:c.4652A>G	NP_001333742.1:p.Gln1551Arg
NM_001363725.1:c.2402A>G	NP_001350654.1:p.Gln801Arg
XM_011535984.2:c.4862A>G	XP_011534286.2:p.Gln1621Arg
XM_011535988.3:c.1793A>G	XP_011534290.1:p.Gln598Arg
XM_017011103.2:c.4763A>G	XP_016866592.1:p.Gln1588Arg
XM_017011104.1:c.4733A>G	XP_016866593.1:p.Gln1578Arg
XM_017011105.2:c.4703A>G	XP_016866594.1:p.Gln1568Arg
XM_017011106.2:c.4574A>G	XP_016866595.1:p.Gln1525Arg
XM_017011107.2:c.4553A>G	XP_016866596.1:p.Gln1518Arg
XR_002956289.1:n.4848A>G
NM_001363725.2:c.2402A>G	NP_001350654.1:p.Gln801Arg
NM_001371656.1:c.4781A>G	NP_001358585.1:p.Gln1594Arg
NM_001374820.1:c.4781A>G	NP_001361749.1:p.Gln1594Arg
NM_001374828.1:c.4901A>G MANE Select	NP_001361757.1:p.Gln1634Arg
NM_017519.3:c.4742A>G	NP_059989.3:p.Gln1581Arg