Canonical Allele Identifier: CA366241346

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522109C>G (hg19) ; chr6:g.157200975C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200975C>G , CM000668.2:g.157200975C>G	GRCh38
NC_000006.11:g.157522109C>G , CM000668.1:g.157522109C>G	GRCh37
NC_000006.10:g.157563801C>G	NCBI36
NG_032093.1:g.428046C>G
NG_032093.2:g.428046C>G
NG_066624.1:g.429950C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4591C>G	ENSP00000055163.8:p.Gln1531Glu
ENST00000414678.8:c.4660C>G	ENSP00000412835.3:p.Gln1554Glu
ENST00000637015.2:c.4879C>G	ENSP00000489729.2:p.Gln1627Glu
ENST00000346085.10:c.4630C>G	ENSP00000344546.5:p.Gln1544Glu
ENST00000350026.10:c.4342C>G	ENSP00000055163.7:p.Gln1448Glu
ENST00000414678.7:c.2908C>G	ENSP00000412835.2:p.Gln970Glu
ENST00000635849.1:c.2071C>G	ENSP00000490948.1:p.Gln691Glu
ENST00000635957.1:c.1702C>G	ENSP00000490385.1:p.Gln568Glu
ENST00000636227.1:n.3213C>G
ENST00000636254.1:n.670C>G
ENST00000636930.2:c.4750C>G MANE Select	ENSP00000490491.2:p.Gln1584Glu
ENST00000636940.1:n.2747C>G
ENST00000637015.1:c.2118C>G
ENST00000637568.1:c.2032C>G
ENST00000637741.1:n.1416C>G
ENST00000637810.1:c.2092C>G	ENSP00000489636.1:p.Gln698Glu
ENST00000637904.1:c.2251C>G	ENSP00000490550.1:p.Gln751Glu
ENST00000647938.1:c.4381C>G	ENSP00000498155.1:p.Gln1461Glu
ENST00000346085.9:c.4381C>G	ENSP00000344546.4:p.Gln1461Glu
ENST00000350026.9:c.4342C>G	ENSP00000055163.7:p.Gln1448Glu
ENST00000414678.6:c.2908C>G	ENSP00000412835.2:p.Gln970Glu
NM_017519.2:c.4342C>G	NP_059989.2:p.Gln1448Glu
NM_020732.3:c.4381C>G	NP_065783.3:p.Gln1461Glu
XM_005267069.3:c.4501C>G	XP_005267126.2:p.Gln1501Glu
XM_011535984.1:c.3580C>G	XP_011534286.1:p.Gln1194Glu
XM_011535985.1:c.3400C>G	XP_011534287.1:p.Gln1134Glu
XM_011535986.1:c.3160C>G	XP_011534288.1:p.Gln1054Glu
XM_011535987.1:c.2779C>G	XP_011534289.1:p.Gln927Glu
XM_011535988.1:c.1642C>G	XP_011534290.1:p.Gln548Glu
NM_001346813.1:c.4501C>G	NP_001333742.1:p.Gln1501Glu
NM_001363725.1:c.2251C>G	NP_001350654.1:p.Gln751Glu
XM_011535984.2:c.4711C>G	XP_011534286.2:p.Gln1571Glu
XM_011535988.3:c.1642C>G	XP_011534290.1:p.Gln548Glu
XM_017011103.2:c.4612C>G	XP_016866592.1:p.Gln1538Glu
XM_017011104.1:c.4582C>G	XP_016866593.1:p.Gln1528Glu
XM_017011105.2:c.4552C>G	XP_016866594.1:p.Gln1518Glu
XM_017011106.2:c.4423C>G	XP_016866595.1:p.Gln1475Glu
XM_017011107.2:c.4402C>G	XP_016866596.1:p.Gln1468Glu
XR_002956289.1:n.4697C>G
NM_001363725.2:c.2251C>G	NP_001350654.1:p.Gln751Glu
NM_001371656.1:c.4630C>G	NP_001358585.1:p.Gln1544Glu
NM_001374820.1:c.4630C>G	NP_001361749.1:p.Gln1544Glu
NM_001374828.1:c.4750C>G MANE Select	NP_001361757.1:p.Gln1584Glu
NM_017519.3:c.4591C>G	NP_059989.3:p.Gln1531Glu