Canonical Allele Identifier: CA366234028

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510793C>G (hg19) ; chr6:g.157189659C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189659C>G , CM000668.2:g.157189659C>G	GRCh38
NC_000006.11:g.157510793C>G , CM000668.1:g.157510793C>G	GRCh37
NC_000006.10:g.157552485C>G	NCBI36
NG_032093.1:g.416730C>G
NG_032093.2:g.416730C>G
NG_066624.1:g.418634C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3778C>G	ENSP00000055163.8:p.Gln1260Glu
ENST00000414678.8:c.3847C>G	ENSP00000412835.3:p.Gln1283Glu
ENST00000637015.2:c.4066C>G	ENSP00000489729.2:p.Gln1356Glu
ENST00000346085.10:c.3817C>G	ENSP00000344546.5:p.Gln1273Glu
ENST00000350026.10:c.3529C>G	ENSP00000055163.7:p.Gln1177Glu
ENST00000414678.7:c.2095C>G	ENSP00000412835.2:p.Gln699Glu
ENST00000635849.1:c.1258C>G	ENSP00000490948.1:p.Gln420Glu
ENST00000635957.1:c.892C>G	ENSP00000490385.1:p.Gln298Glu
ENST00000636930.2:c.3937C>G MANE Select	ENSP00000490491.2:p.Gln1313Glu
ENST00000636940.1:n.1934C>G
ENST00000637015.1:c.1305C>G
ENST00000637568.1:c.1219C>G
ENST00000637741.1:n.603C>G
ENST00000637810.1:c.1279C>G	ENSP00000489636.1:p.Gln427Glu
ENST00000637904.1:c.1438C>G	ENSP00000490550.1:p.Gln480Glu
ENST00000647938.1:c.3568C>G	ENSP00000498155.1:p.Gln1190Glu
ENST00000346085.9:c.3568C>G	ENSP00000344546.4:p.Gln1190Glu
ENST00000350026.9:c.3529C>G	ENSP00000055163.7:p.Gln1177Glu
ENST00000414678.6:c.2095C>G	ENSP00000412835.2:p.Gln699Glu
NM_017519.2:c.3529C>G	NP_059989.2:p.Gln1177Glu
NM_020732.3:c.3568C>G	NP_065783.3:p.Gln1190Glu
XM_005267069.3:c.3688C>G	XP_005267126.2:p.Gln1230Glu
XM_011535984.1:c.2767C>G	XP_011534286.1:p.Gln923Glu
XM_011535985.1:c.2587C>G	XP_011534287.1:p.Gln863Glu
XM_011535986.1:c.2347C>G	XP_011534288.1:p.Gln783Glu
XM_011535987.1:c.1966C>G	XP_011534289.1:p.Gln656Glu
XM_011535988.1:c.829C>G	XP_011534290.1:p.Gln277Glu
NM_001346813.1:c.3688C>G	NP_001333742.1:p.Gln1230Glu
NM_001363725.1:c.1438C>G	NP_001350654.1:p.Gln480Glu
XM_011535984.2:c.3898C>G	XP_011534286.2:p.Gln1300Glu
XM_011535988.3:c.829C>G	XP_011534290.1:p.Gln277Glu
XM_017011103.2:c.3799C>G	XP_016866592.1:p.Gln1267Glu
XM_017011104.1:c.3769C>G	XP_016866593.1:p.Gln1257Glu
XM_017011105.2:c.3739C>G	XP_016866594.1:p.Gln1247Glu
XM_017011106.2:c.3610C>G	XP_016866595.1:p.Gln1204Glu
XM_017011107.2:c.3589C>G	XP_016866596.1:p.Gln1197Glu
XR_002956289.1:n.3981C>G
NM_001363725.2:c.1438C>G	NP_001350654.1:p.Gln480Glu
NM_001371656.1:c.3817C>G	NP_001358585.1:p.Gln1273Glu
NM_001374820.1:c.3817C>G	NP_001361749.1:p.Gln1273Glu
NM_001374828.1:c.3937C>G MANE Select	NP_001361757.1:p.Gln1313Glu
NM_017519.3:c.3778C>G	NP_059989.3:p.Gln1260Glu