Canonical Allele Identifier: CA366242762

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522500A>G (hg19) ; chr6:g.157201366A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201366A>G , CM000668.2:g.157201366A>G	GRCh38
NC_000006.11:g.157522500A>G , CM000668.1:g.157522500A>G	GRCh37
NC_000006.10:g.157564192A>G	NCBI36
NG_032093.1:g.428437A>G
NG_032093.2:g.428437A>G
NG_066624.1:g.430341A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4982A>G	ENSP00000055163.8:p.Gln1661Arg
ENST00000414678.8:c.5051A>G	ENSP00000412835.3:p.Gln1684Arg
ENST00000637015.2:c.5270A>G	ENSP00000489729.2:p.Gln1757Arg
ENST00000346085.10:c.5021A>G	ENSP00000344546.5:p.Gln1674Arg
ENST00000350026.10:c.4733A>G	ENSP00000055163.7:p.Gln1578Arg
ENST00000414678.7:c.3299A>G	ENSP00000412835.2:p.Gln1100Arg
ENST00000635849.1:c.2462A>G	ENSP00000490948.1:p.Gln821Arg
ENST00000635957.1:c.2093A>G	ENSP00000490385.1:p.Gln698Arg
ENST00000636227.1:n.3604A>G
ENST00000636254.1:n.1061A>G
ENST00000636930.2:c.5141A>G MANE Select	ENSP00000490491.2:p.Gln1714Arg
ENST00000636940.1:n.3138A>G
ENST00000637015.1:c.2509A>G
ENST00000637568.1:c.2423A>G
ENST00000637741.1:n.1807A>G
ENST00000637810.1:c.2483A>G	ENSP00000489636.1:p.Gln828Arg
ENST00000637904.1:c.2642A>G	ENSP00000490550.1:p.Gln881Arg
ENST00000647938.1:c.4772A>G	ENSP00000498155.1:p.Gln1591Arg
ENST00000346085.9:c.4772A>G	ENSP00000344546.4:p.Gln1591Arg
ENST00000350026.9:c.4733A>G	ENSP00000055163.7:p.Gln1578Arg
ENST00000414678.6:c.3299A>G	ENSP00000412835.2:p.Gln1100Arg
NM_017519.2:c.4733A>G	NP_059989.2:p.Gln1578Arg
NM_020732.3:c.4772A>G	NP_065783.3:p.Gln1591Arg
XM_005267069.3:c.4892A>G	XP_005267126.2:p.Gln1631Arg
XM_011535984.1:c.3971A>G	XP_011534286.1:p.Gln1324Arg
XM_011535985.1:c.3791A>G	XP_011534287.1:p.Gln1264Arg
XM_011535986.1:c.3551A>G	XP_011534288.1:p.Gln1184Arg
XM_011535987.1:c.3170A>G	XP_011534289.1:p.Gln1057Arg
XM_011535988.1:c.2033A>G	XP_011534290.1:p.Gln678Arg
NM_001346813.1:c.4892A>G	NP_001333742.1:p.Gln1631Arg
NM_001363725.1:c.2642A>G	NP_001350654.1:p.Gln881Arg
XM_011535984.2:c.5102A>G	XP_011534286.2:p.Gln1701Arg
XM_011535988.3:c.2033A>G	XP_011534290.1:p.Gln678Arg
XM_017011103.2:c.5003A>G	XP_016866592.1:p.Gln1668Arg
XM_017011104.1:c.4973A>G	XP_016866593.1:p.Gln1658Arg
XM_017011105.2:c.4943A>G	XP_016866594.1:p.Gln1648Arg
XM_017011106.2:c.4814A>G	XP_016866595.1:p.Gln1605Arg
XM_017011107.2:c.4793A>G	XP_016866596.1:p.Gln1598Arg
XR_002956289.1:n.5088A>G
NM_001363725.2:c.2642A>G	NP_001350654.1:p.Gln881Arg
NM_001371656.1:c.5021A>G	NP_001358585.1:p.Gln1674Arg
NM_001374820.1:c.5021A>G	NP_001361749.1:p.Gln1674Arg
NM_001374828.1:c.5141A>G MANE Select	NP_001361757.1:p.Gln1714Arg
NM_017519.3:c.4982A>G	NP_059989.3:p.Gln1661Arg