Canonical Allele Identifier: CA366234027

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554232919
• MyVariant Identifiers: chr6:g.157510793C>A (hg19) ; chr6:g.157189659C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3778C>A	ENSP00000055163.8:p.Gln1260Lys
ENST00000414678.8:c.3847C>A	ENSP00000412835.3:p.Gln1283Lys
ENST00000637015.2:c.4066C>A	ENSP00000489729.2:p.Gln1356Lys
ENST00000346085.10:c.3817C>A	ENSP00000344546.5:p.Gln1273Lys
ENST00000350026.10:c.3529C>A	ENSP00000055163.7:p.Gln1177Lys
ENST00000414678.7:c.2095C>A	ENSP00000412835.2:p.Gln699Lys
ENST00000635849.1:c.1258C>A	ENSP00000490948.1:p.Gln420Lys
ENST00000635957.1:c.892C>A	ENSP00000490385.1:p.Gln298Lys
ENST00000636930.2:c.3937C>A MANE Select	ENSP00000490491.2:p.Gln1313Lys
ENST00000636940.1:n.1934C>A
ENST00000637015.1:c.1305C>A
ENST00000637568.1:c.1219C>A
ENST00000637741.1:n.603C>A
ENST00000637810.1:c.1279C>A	ENSP00000489636.1:p.Gln427Lys
ENST00000637904.1:c.1438C>A	ENSP00000490550.1:p.Gln480Lys
ENST00000647938.1:c.3568C>A	ENSP00000498155.1:p.Gln1190Lys
ENST00000346085.9:c.3568C>A	ENSP00000344546.4:p.Gln1190Lys
ENST00000350026.9:c.3529C>A	ENSP00000055163.7:p.Gln1177Lys
ENST00000414678.6:c.2095C>A	ENSP00000412835.2:p.Gln699Lys
NM_017519.2:c.3529C>A	NP_059989.2:p.Gln1177Lys
NM_020732.3:c.3568C>A	NP_065783.3:p.Gln1190Lys
XM_005267069.3:c.3688C>A	XP_005267126.2:p.Gln1230Lys
XM_011535984.1:c.2767C>A	XP_011534286.1:p.Gln923Lys
XM_011535985.1:c.2587C>A	XP_011534287.1:p.Gln863Lys
XM_011535986.1:c.2347C>A	XP_011534288.1:p.Gln783Lys
XM_011535987.1:c.1966C>A	XP_011534289.1:p.Gln656Lys
XM_011535988.1:c.829C>A	XP_011534290.1:p.Gln277Lys
NM_001346813.1:c.3688C>A	NP_001333742.1:p.Gln1230Lys
NM_001363725.1:c.1438C>A	NP_001350654.1:p.Gln480Lys
XM_011535984.2:c.3898C>A	XP_011534286.2:p.Gln1300Lys
XM_011535988.3:c.829C>A	XP_011534290.1:p.Gln277Lys
XM_017011103.2:c.3799C>A	XP_016866592.1:p.Gln1267Lys
XM_017011104.1:c.3769C>A	XP_016866593.1:p.Gln1257Lys
XM_017011105.2:c.3739C>A	XP_016866594.1:p.Gln1247Lys
XM_017011106.2:c.3610C>A	XP_016866595.1:p.Gln1204Lys
XM_017011107.2:c.3589C>A	XP_016866596.1:p.Gln1197Lys
XR_002956289.1:n.3981C>A
NM_001363725.2:c.1438C>A	NP_001350654.1:p.Gln480Lys
NM_001371656.1:c.3817C>A	NP_001358585.1:p.Gln1273Lys
NM_001374820.1:c.3817C>A	NP_001361749.1:p.Gln1273Lys
NM_001374828.1:c.3937C>A MANE Select	NP_001361757.1:p.Gln1313Lys
NM_017519.3:c.3778C>A	NP_059989.3:p.Gln1260Lys