Canonical Allele Identifier: CA366242617

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522471G>T (hg19) ; chr6:g.157201337G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201337G>T , CM000668.2:g.157201337G>T	GRCh38
NC_000006.11:g.157522471G>T , CM000668.1:g.157522471G>T	GRCh37
NC_000006.10:g.157564163G>T	NCBI36
NG_032093.1:g.428408G>T
NG_032093.2:g.428408G>T
NG_066624.1:g.430312G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4953G>T	ENSP00000055163.8:p.Gln1651His
ENST00000414678.8:c.5022G>T	ENSP00000412835.3:p.Gln1674His
ENST00000637015.2:c.5241G>T	ENSP00000489729.2:p.Gln1747His
ENST00000346085.10:c.4992G>T	ENSP00000344546.5:p.Gln1664His
ENST00000350026.10:c.4704G>T	ENSP00000055163.7:p.Gln1568His
ENST00000414678.7:c.3270G>T	ENSP00000412835.2:p.Gln1090His
ENST00000635849.1:c.2433G>T	ENSP00000490948.1:p.Gln811His
ENST00000635957.1:c.2064G>T	ENSP00000490385.1:p.Gln688His
ENST00000636227.1:n.3575G>T
ENST00000636254.1:n.1032G>T
ENST00000636930.2:c.5112G>T MANE Select	ENSP00000490491.2:p.Gln1704His
ENST00000636940.1:n.3109G>T
ENST00000637015.1:c.2480G>T
ENST00000637568.1:c.2394G>T
ENST00000637741.1:n.1778G>T
ENST00000637810.1:c.2454G>T	ENSP00000489636.1:p.Gln818His
ENST00000637904.1:c.2613G>T	ENSP00000490550.1:p.Gln871His
ENST00000647938.1:c.4743G>T	ENSP00000498155.1:p.Gln1581His
ENST00000346085.9:c.4743G>T	ENSP00000344546.4:p.Gln1581His
ENST00000350026.9:c.4704G>T	ENSP00000055163.7:p.Gln1568His
ENST00000414678.6:c.3270G>T	ENSP00000412835.2:p.Gln1090His
NM_017519.2:c.4704G>T	NP_059989.2:p.Gln1568His
NM_020732.3:c.4743G>T	NP_065783.3:p.Gln1581His
XM_005267069.3:c.4863G>T	XP_005267126.2:p.Gln1621His
XM_011535984.1:c.3942G>T	XP_011534286.1:p.Gln1314His
XM_011535985.1:c.3762G>T	XP_011534287.1:p.Gln1254His
XM_011535986.1:c.3522G>T	XP_011534288.1:p.Gln1174His
XM_011535987.1:c.3141G>T	XP_011534289.1:p.Gln1047His
XM_011535988.1:c.2004G>T	XP_011534290.1:p.Gln668His
NM_001346813.1:c.4863G>T	NP_001333742.1:p.Gln1621His
NM_001363725.1:c.2613G>T	NP_001350654.1:p.Gln871His
XM_011535984.2:c.5073G>T	XP_011534286.2:p.Gln1691His
XM_011535988.3:c.2004G>T	XP_011534290.1:p.Gln668His
XM_017011103.2:c.4974G>T	XP_016866592.1:p.Gln1658His
XM_017011104.1:c.4944G>T	XP_016866593.1:p.Gln1648His
XM_017011105.2:c.4914G>T	XP_016866594.1:p.Gln1638His
XM_017011106.2:c.4785G>T	XP_016866595.1:p.Gln1595His
XM_017011107.2:c.4764G>T	XP_016866596.1:p.Gln1588His
XR_002956289.1:n.5059G>T
NM_001363725.2:c.2613G>T	NP_001350654.1:p.Gln871His
NM_001371656.1:c.4992G>T	NP_001358585.1:p.Gln1664His
NM_001374820.1:c.4992G>T	NP_001361749.1:p.Gln1664His
NM_001374828.1:c.5112G>T MANE Select	NP_001361757.1:p.Gln1704His
NM_017519.3:c.4953G>T	NP_059989.3:p.Gln1651His