Canonical Allele Identifier: CA366241349

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794064071
• MyVariant Identifiers: chr6:g.157522110A>G (hg19) ; chr6:g.157200976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200976A>G , CM000668.2:g.157200976A>G	GRCh38
NC_000006.11:g.157522110A>G , CM000668.1:g.157522110A>G	GRCh37
NC_000006.10:g.157563802A>G	NCBI36
NG_032093.1:g.428047A>G
NG_032093.2:g.428047A>G
NG_066624.1:g.429951A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4592A>G	ENSP00000055163.8:p.Gln1531Arg
ENST00000414678.8:c.4661A>G	ENSP00000412835.3:p.Gln1554Arg
ENST00000637015.2:c.4880A>G	ENSP00000489729.2:p.Gln1627Arg
ENST00000346085.10:c.4631A>G	ENSP00000344546.5:p.Gln1544Arg
ENST00000350026.10:c.4343A>G	ENSP00000055163.7:p.Gln1448Arg
ENST00000414678.7:c.2909A>G	ENSP00000412835.2:p.Gln970Arg
ENST00000635849.1:c.2072A>G	ENSP00000490948.1:p.Gln691Arg
ENST00000635957.1:c.1703A>G	ENSP00000490385.1:p.Gln568Arg
ENST00000636227.1:n.3214A>G
ENST00000636254.1:n.671A>G
ENST00000636930.2:c.4751A>G MANE Select	ENSP00000490491.2:p.Gln1584Arg
ENST00000636940.1:n.2748A>G
ENST00000637015.1:c.2119A>G
ENST00000637568.1:c.2033A>G
ENST00000637741.1:n.1417A>G
ENST00000637810.1:c.2093A>G	ENSP00000489636.1:p.Gln698Arg
ENST00000637904.1:c.2252A>G	ENSP00000490550.1:p.Gln751Arg
ENST00000647938.1:c.4382A>G	ENSP00000498155.1:p.Gln1461Arg
ENST00000346085.9:c.4382A>G	ENSP00000344546.4:p.Gln1461Arg
ENST00000350026.9:c.4343A>G	ENSP00000055163.7:p.Gln1448Arg
ENST00000414678.6:c.2909A>G	ENSP00000412835.2:p.Gln970Arg
NM_017519.2:c.4343A>G	NP_059989.2:p.Gln1448Arg
NM_020732.3:c.4382A>G	NP_065783.3:p.Gln1461Arg
XM_005267069.3:c.4502A>G	XP_005267126.2:p.Gln1501Arg
XM_011535984.1:c.3581A>G	XP_011534286.1:p.Gln1194Arg
XM_011535985.1:c.3401A>G	XP_011534287.1:p.Gln1134Arg
XM_011535986.1:c.3161A>G	XP_011534288.1:p.Gln1054Arg
XM_011535987.1:c.2780A>G	XP_011534289.1:p.Gln927Arg
XM_011535988.1:c.1643A>G	XP_011534290.1:p.Gln548Arg
NM_001346813.1:c.4502A>G	NP_001333742.1:p.Gln1501Arg
NM_001363725.1:c.2252A>G	NP_001350654.1:p.Gln751Arg
XM_011535984.2:c.4712A>G	XP_011534286.2:p.Gln1571Arg
XM_011535988.3:c.1643A>G	XP_011534290.1:p.Gln548Arg
XM_017011103.2:c.4613A>G	XP_016866592.1:p.Gln1538Arg
XM_017011104.1:c.4583A>G	XP_016866593.1:p.Gln1528Arg
XM_017011105.2:c.4553A>G	XP_016866594.1:p.Gln1518Arg
XM_017011106.2:c.4424A>G	XP_016866595.1:p.Gln1475Arg
XM_017011107.2:c.4403A>G	XP_016866596.1:p.Gln1468Arg
XR_002956289.1:n.4698A>G
NM_001363725.2:c.2252A>G	NP_001350654.1:p.Gln751Arg
NM_001371656.1:c.4631A>G	NP_001358585.1:p.Gln1544Arg
NM_001374820.1:c.4631A>G	NP_001361749.1:p.Gln1544Arg
NM_001374828.1:c.4751A>G MANE Select	NP_001361757.1:p.Gln1584Arg
NM_017519.3:c.4592A>G	NP_059989.3:p.Gln1531Arg