Canonical Allele Identifier: CA366234029

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 689741
• ClinVar RCV Id: RCV000850528 ; RCV001533120
• dbSNP Id: rs1554232919
• MyVariant Identifiers: chr6:g.157510793C>T (hg19) ; chr6:g.157189659C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3778C>T	ENSP00000055163.8:p.Gln1260Ter
ENST00000414678.8:c.3847C>T	ENSP00000412835.3:p.Gln1283Ter
ENST00000637015.2:c.4066C>T	ENSP00000489729.2:p.Gln1356Ter
ENST00000346085.10:c.3817C>T	ENSP00000344546.5:p.Gln1273Ter
ENST00000350026.10:c.3529C>T	ENSP00000055163.7:p.Gln1177Ter
ENST00000414678.7:c.2095C>T	ENSP00000412835.2:p.Gln699Ter
ENST00000635849.1:c.1258C>T	ENSP00000490948.1:p.Gln420Ter
ENST00000635957.1:c.892C>T	ENSP00000490385.1:p.Gln298Ter
ENST00000636930.2:c.3937C>T MANE Select	ENSP00000490491.2:p.Gln1313Ter
ENST00000636940.1:n.1934C>T
ENST00000637015.1:c.1305C>T
ENST00000637568.1:c.1219C>T
ENST00000637741.1:n.603C>T
ENST00000637810.1:c.1279C>T	ENSP00000489636.1:p.Gln427Ter
ENST00000637904.1:c.1438C>T	ENSP00000490550.1:p.Gln480Ter
ENST00000647938.1:c.3568C>T	ENSP00000498155.1:p.Gln1190Ter
ENST00000346085.9:c.3568C>T	ENSP00000344546.4:p.Gln1190Ter
ENST00000350026.9:c.3529C>T	ENSP00000055163.7:p.Gln1177Ter
ENST00000414678.6:c.2095C>T	ENSP00000412835.2:p.Gln699Ter
NM_017519.2:c.3529C>T	NP_059989.2:p.Gln1177Ter
NM_020732.3:c.3568C>T	NP_065783.3:p.Gln1190Ter
XM_005267069.3:c.3688C>T	XP_005267126.2:p.Gln1230Ter
XM_011535984.1:c.2767C>T	XP_011534286.1:p.Gln923Ter
XM_011535985.1:c.2587C>T	XP_011534287.1:p.Gln863Ter
XM_011535986.1:c.2347C>T	XP_011534288.1:p.Gln783Ter
XM_011535987.1:c.1966C>T	XP_011534289.1:p.Gln656Ter
XM_011535988.1:c.829C>T	XP_011534290.1:p.Gln277Ter
NM_001346813.1:c.3688C>T	NP_001333742.1:p.Gln1230Ter
NM_001363725.1:c.1438C>T	NP_001350654.1:p.Gln480Ter
XM_011535984.2:c.3898C>T	XP_011534286.2:p.Gln1300Ter
XM_011535988.3:c.829C>T	XP_011534290.1:p.Gln277Ter
XM_017011103.2:c.3799C>T	XP_016866592.1:p.Gln1267Ter
XM_017011104.1:c.3769C>T	XP_016866593.1:p.Gln1257Ter
XM_017011105.2:c.3739C>T	XP_016866594.1:p.Gln1247Ter
XM_017011106.2:c.3610C>T	XP_016866595.1:p.Gln1204Ter
XM_017011107.2:c.3589C>T	XP_016866596.1:p.Gln1197Ter
XR_002956289.1:n.3981C>T
NM_001363725.2:c.1438C>T	NP_001350654.1:p.Gln480Ter
NM_001371656.1:c.3817C>T	NP_001358585.1:p.Gln1273Ter
NM_001374820.1:c.3817C>T	NP_001361749.1:p.Gln1273Ter
NM_001374828.1:c.3937C>T MANE Select	NP_001361757.1:p.Gln1313Ter
NM_017519.3:c.3778C>T	NP_059989.3:p.Gln1260Ter