Canonical Allele Identifier: CA366242614

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522470A>G (hg19) ; chr6:g.157201336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201336A>G , CM000668.2:g.157201336A>G	GRCh38
NC_000006.11:g.157522470A>G , CM000668.1:g.157522470A>G	GRCh37
NC_000006.10:g.157564162A>G	NCBI36
NG_032093.1:g.428407A>G
NG_032093.2:g.428407A>G
NG_066624.1:g.430311A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4952A>G	ENSP00000055163.8:p.Gln1651Arg
ENST00000414678.8:c.5021A>G	ENSP00000412835.3:p.Gln1674Arg
ENST00000637015.2:c.5240A>G	ENSP00000489729.2:p.Gln1747Arg
ENST00000346085.10:c.4991A>G	ENSP00000344546.5:p.Gln1664Arg
ENST00000350026.10:c.4703A>G	ENSP00000055163.7:p.Gln1568Arg
ENST00000414678.7:c.3269A>G	ENSP00000412835.2:p.Gln1090Arg
ENST00000635849.1:c.2432A>G	ENSP00000490948.1:p.Gln811Arg
ENST00000635957.1:c.2063A>G	ENSP00000490385.1:p.Gln688Arg
ENST00000636227.1:n.3574A>G
ENST00000636254.1:n.1031A>G
ENST00000636930.2:c.5111A>G MANE Select	ENSP00000490491.2:p.Gln1704Arg
ENST00000636940.1:n.3108A>G
ENST00000637015.1:c.2479A>G
ENST00000637568.1:c.2393A>G
ENST00000637741.1:n.1777A>G
ENST00000637810.1:c.2453A>G	ENSP00000489636.1:p.Gln818Arg
ENST00000637904.1:c.2612A>G	ENSP00000490550.1:p.Gln871Arg
ENST00000647938.1:c.4742A>G	ENSP00000498155.1:p.Gln1581Arg
ENST00000346085.9:c.4742A>G	ENSP00000344546.4:p.Gln1581Arg
ENST00000350026.9:c.4703A>G	ENSP00000055163.7:p.Gln1568Arg
ENST00000414678.6:c.3269A>G	ENSP00000412835.2:p.Gln1090Arg
NM_017519.2:c.4703A>G	NP_059989.2:p.Gln1568Arg
NM_020732.3:c.4742A>G	NP_065783.3:p.Gln1581Arg
XM_005267069.3:c.4862A>G	XP_005267126.2:p.Gln1621Arg
XM_011535984.1:c.3941A>G	XP_011534286.1:p.Gln1314Arg
XM_011535985.1:c.3761A>G	XP_011534287.1:p.Gln1254Arg
XM_011535986.1:c.3521A>G	XP_011534288.1:p.Gln1174Arg
XM_011535987.1:c.3140A>G	XP_011534289.1:p.Gln1047Arg
XM_011535988.1:c.2003A>G	XP_011534290.1:p.Gln668Arg
NM_001346813.1:c.4862A>G	NP_001333742.1:p.Gln1621Arg
NM_001363725.1:c.2612A>G	NP_001350654.1:p.Gln871Arg
XM_011535984.2:c.5072A>G	XP_011534286.2:p.Gln1691Arg
XM_011535988.3:c.2003A>G	XP_011534290.1:p.Gln668Arg
XM_017011103.2:c.4973A>G	XP_016866592.1:p.Gln1658Arg
XM_017011104.1:c.4943A>G	XP_016866593.1:p.Gln1648Arg
XM_017011105.2:c.4913A>G	XP_016866594.1:p.Gln1638Arg
XM_017011106.2:c.4784A>G	XP_016866595.1:p.Gln1595Arg
XM_017011107.2:c.4763A>G	XP_016866596.1:p.Gln1588Arg
XR_002956289.1:n.5058A>G
NM_001363725.2:c.2612A>G	NP_001350654.1:p.Gln871Arg
NM_001371656.1:c.4991A>G	NP_001358585.1:p.Gln1664Arg
NM_001374820.1:c.4991A>G	NP_001361749.1:p.Gln1664Arg
NM_001374828.1:c.5111A>G MANE Select	NP_001361757.1:p.Gln1704Arg
NM_017519.3:c.4952A>G	NP_059989.3:p.Gln1651Arg