Canonical Allele Identifier: CA366234242

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510890A>G (hg19) ; chr6:g.157189756A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189756A>G , CM000668.2:g.157189756A>G	GRCh38
NC_000006.11:g.157510890A>G , CM000668.1:g.157510890A>G	GRCh37
NC_000006.10:g.157552582A>G	NCBI36
NG_032093.1:g.416827A>G
NG_032093.2:g.416827A>G
NG_066624.1:g.418731A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3875A>G	ENSP00000055163.8:p.Gln1292Arg
ENST00000414678.8:c.3944A>G	ENSP00000412835.3:p.Gln1315Arg
ENST00000637015.2:c.4163A>G	ENSP00000489729.2:p.Gln1388Arg
ENST00000346085.10:c.3914A>G	ENSP00000344546.5:p.Gln1305Arg
ENST00000350026.10:c.3626A>G	ENSP00000055163.7:p.Gln1209Arg
ENST00000414678.7:c.2192A>G	ENSP00000412835.2:p.Gln731Arg
ENST00000635849.1:c.1355A>G	ENSP00000490948.1:p.Gln452Arg
ENST00000635957.1:c.989A>G	ENSP00000490385.1:p.Gln330Arg
ENST00000636930.2:c.4034A>G MANE Select	ENSP00000490491.2:p.Gln1345Arg
ENST00000636940.1:n.2031A>G
ENST00000637015.1:c.1402A>G
ENST00000637568.1:c.1316A>G
ENST00000637741.1:n.700A>G
ENST00000637810.1:c.1376A>G	ENSP00000489636.1:p.Gln459Arg
ENST00000637904.1:c.1535A>G	ENSP00000490550.1:p.Gln512Arg
ENST00000647938.1:c.3665A>G	ENSP00000498155.1:p.Gln1222Arg
ENST00000346085.9:c.3665A>G	ENSP00000344546.4:p.Gln1222Arg
ENST00000350026.9:c.3626A>G	ENSP00000055163.7:p.Gln1209Arg
ENST00000414678.6:c.2192A>G	ENSP00000412835.2:p.Gln731Arg
NM_017519.2:c.3626A>G	NP_059989.2:p.Gln1209Arg
NM_020732.3:c.3665A>G	NP_065783.3:p.Gln1222Arg
XM_005267069.3:c.3785A>G	XP_005267126.2:p.Gln1262Arg
XM_011535984.1:c.2864A>G	XP_011534286.1:p.Gln955Arg
XM_011535985.1:c.2684A>G	XP_011534287.1:p.Gln895Arg
XM_011535986.1:c.2444A>G	XP_011534288.1:p.Gln815Arg
XM_011535987.1:c.2063A>G	XP_011534289.1:p.Gln688Arg
XM_011535988.1:c.926A>G	XP_011534290.1:p.Gln309Arg
NM_001346813.1:c.3785A>G	NP_001333742.1:p.Gln1262Arg
NM_001363725.1:c.1535A>G	NP_001350654.1:p.Gln512Arg
XM_011535984.2:c.3995A>G	XP_011534286.2:p.Gln1332Arg
XM_011535988.3:c.926A>G	XP_011534290.1:p.Gln309Arg
XM_017011103.2:c.3896A>G	XP_016866592.1:p.Gln1299Arg
XM_017011104.1:c.3866A>G	XP_016866593.1:p.Gln1289Arg
XM_017011105.2:c.3836A>G	XP_016866594.1:p.Gln1279Arg
XM_017011106.2:c.3707A>G	XP_016866595.1:p.Gln1236Arg
XM_017011107.2:c.3686A>G	XP_016866596.1:p.Gln1229Arg
XR_002956289.1:n.4078A>G
NM_001363725.2:c.1535A>G	NP_001350654.1:p.Gln512Arg
NM_001371656.1:c.3914A>G	NP_001358585.1:p.Gln1305Arg
NM_001374820.1:c.3914A>G	NP_001361749.1:p.Gln1305Arg
NM_001374828.1:c.4034A>G MANE Select	NP_001361757.1:p.Gln1345Arg
NM_017519.3:c.3875A>G	NP_059989.3:p.Gln1292Arg