Canonical Allele Identifier: CA366239572

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366055
• MyVariant Identifiers: chr6:g.157519965A>G (hg19) ; chr6:g.157198831A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198831A>G , CM000668.2:g.157198831A>G	GRCh38
NC_000006.11:g.157519965A>G , CM000668.1:g.157519965A>G	GRCh37
NC_000006.10:g.157561657A>G	NCBI36
NG_032093.1:g.425902A>G
NG_032093.2:g.425902A>G
NG_066624.1:g.427806A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4244A>G	ENSP00000055163.8:p.Gln1415Arg
ENST00000414678.8:c.4313A>G	ENSP00000412835.3:p.Gln1438Arg
ENST00000637015.2:c.4532A>G	ENSP00000489729.2:p.Gln1511Arg
ENST00000346085.10:c.4283A>G	ENSP00000344546.5:p.Gln1428Arg
ENST00000350026.10:c.3995A>G	ENSP00000055163.7:p.Gln1332Arg
ENST00000414678.7:c.2561A>G	ENSP00000412835.2:p.Gln854Arg
ENST00000635849.1:c.1724A>G	ENSP00000490948.1:p.Gln575Arg
ENST00000635957.1:c.1355A>G	ENSP00000490385.1:p.Gln452Arg
ENST00000636227.1:n.2866A>G
ENST00000636254.1:n.323A>G
ENST00000636930.2:c.4403A>G MANE Select	ENSP00000490491.2:p.Gln1468Arg
ENST00000636940.1:n.2400A>G
ENST00000637015.1:c.1771A>G
ENST00000637568.1:c.1685A>G
ENST00000637741.1:n.1069A>G
ENST00000637810.1:c.1745A>G	ENSP00000489636.1:p.Gln582Arg
ENST00000637904.1:c.1904A>G	ENSP00000490550.1:p.Gln635Arg
ENST00000647938.1:c.4034A>G	ENSP00000498155.1:p.Gln1345Arg
ENST00000346085.9:c.4034A>G	ENSP00000344546.4:p.Gln1345Arg
ENST00000350026.9:c.3995A>G	ENSP00000055163.7:p.Gln1332Arg
ENST00000414678.6:c.2561A>G	ENSP00000412835.2:p.Gln854Arg
NM_017519.2:c.3995A>G	NP_059989.2:p.Gln1332Arg
NM_020732.3:c.4034A>G	NP_065783.3:p.Gln1345Arg
XM_005267069.3:c.4154A>G	XP_005267126.2:p.Gln1385Arg
XM_011535984.1:c.3233A>G	XP_011534286.1:p.Gln1078Arg
XM_011535985.1:c.3053A>G	XP_011534287.1:p.Gln1018Arg
XM_011535986.1:c.2813A>G	XP_011534288.1:p.Gln938Arg
XM_011535987.1:c.2432A>G	XP_011534289.1:p.Gln811Arg
XM_011535988.1:c.1295A>G	XP_011534290.1:p.Gln432Arg
NM_001346813.1:c.4154A>G	NP_001333742.1:p.Gln1385Arg
NM_001363725.1:c.1904A>G	NP_001350654.1:p.Gln635Arg
XM_011535984.2:c.4364A>G	XP_011534286.2:p.Gln1455Arg
XM_011535988.3:c.1295A>G	XP_011534290.1:p.Gln432Arg
XM_017011103.2:c.4265A>G	XP_016866592.1:p.Gln1422Arg
XM_017011104.1:c.4235A>G	XP_016866593.1:p.Gln1412Arg
XM_017011105.2:c.4205A>G	XP_016866594.1:p.Gln1402Arg
XM_017011106.2:c.4076A>G	XP_016866595.1:p.Gln1359Arg
XM_017011107.2:c.4055A>G	XP_016866596.1:p.Gln1352Arg
XR_002956289.1:n.4427-1874A>G
NM_001363725.2:c.1904A>G	NP_001350654.1:p.Gln635Arg
NM_001371656.1:c.4283A>G	NP_001358585.1:p.Gln1428Arg
NM_001374820.1:c.4283A>G	NP_001361749.1:p.Gln1428Arg
NM_001374828.1:c.4403A>G MANE Select	NP_001361757.1:p.Gln1468Arg
NM_017519.3:c.4244A>G	NP_059989.3:p.Gln1415Arg