Canonical Allele Identifier: CA366242798

Gene: ARID1B

Linked Data

• dbSNP Id: rs910598795
• MyVariant Identifiers: chr6:g.157522506C>T (hg19) ; chr6:g.157201372C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201372C>T , CM000668.2:g.157201372C>T	GRCh38
NC_000006.11:g.157522506C>T , CM000668.1:g.157522506C>T	GRCh37
NC_000006.10:g.157564198C>T	NCBI36
NG_032093.1:g.428443C>T
NG_032093.2:g.428443C>T
NG_066624.1:g.430347C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4988C>T	ENSP00000055163.8:p.Thr1663Ile
ENST00000414678.8:c.5057C>T	ENSP00000412835.3:p.Thr1686Ile
ENST00000637015.2:c.5276C>T	ENSP00000489729.2:p.Thr1759Ile
ENST00000346085.10:c.5027C>T	ENSP00000344546.5:p.Thr1676Ile
ENST00000350026.10:c.4739C>T	ENSP00000055163.7:p.Thr1580Ile
ENST00000414678.7:c.3305C>T	ENSP00000412835.2:p.Thr1102Ile
ENST00000635849.1:c.2468C>T	ENSP00000490948.1:p.Thr823Ile
ENST00000635957.1:c.2099C>T	ENSP00000490385.1:p.Thr700Ile
ENST00000636227.1:n.3610C>T
ENST00000636254.1:n.1067C>T
ENST00000636930.2:c.5147C>T MANE Select	ENSP00000490491.2:p.Thr1716Ile
ENST00000636940.1:n.3144C>T
ENST00000637015.1:c.2515C>T
ENST00000637568.1:c.2429C>T
ENST00000637741.1:n.1813C>T
ENST00000637810.1:c.2489C>T	ENSP00000489636.1:p.Thr830Ile
ENST00000637904.1:c.2648C>T	ENSP00000490550.1:p.Thr883Ile
ENST00000647938.1:c.4778C>T	ENSP00000498155.1:p.Thr1593Ile
ENST00000346085.9:c.4778C>T	ENSP00000344546.4:p.Thr1593Ile
ENST00000350026.9:c.4739C>T	ENSP00000055163.7:p.Thr1580Ile
ENST00000414678.6:c.3305C>T	ENSP00000412835.2:p.Thr1102Ile
NM_017519.2:c.4739C>T	NP_059989.2:p.Thr1580Ile
NM_020732.3:c.4778C>T	NP_065783.3:p.Thr1593Ile
XM_005267069.3:c.4898C>T	XP_005267126.2:p.Thr1633Ile
XM_011535984.1:c.3977C>T	XP_011534286.1:p.Thr1326Ile
XM_011535985.1:c.3797C>T	XP_011534287.1:p.Thr1266Ile
XM_011535986.1:c.3557C>T	XP_011534288.1:p.Thr1186Ile
XM_011535987.1:c.3176C>T	XP_011534289.1:p.Thr1059Ile
XM_011535988.1:c.2039C>T	XP_011534290.1:p.Thr680Ile
NM_001346813.1:c.4898C>T	NP_001333742.1:p.Thr1633Ile
NM_001363725.1:c.2648C>T	NP_001350654.1:p.Thr883Ile
XM_011535984.2:c.5108C>T	XP_011534286.2:p.Thr1703Ile
XM_011535988.3:c.2039C>T	XP_011534290.1:p.Thr680Ile
XM_017011103.2:c.5009C>T	XP_016866592.1:p.Thr1670Ile
XM_017011104.1:c.4979C>T	XP_016866593.1:p.Thr1660Ile
XM_017011105.2:c.4949C>T	XP_016866594.1:p.Thr1650Ile
XM_017011106.2:c.4820C>T	XP_016866595.1:p.Thr1607Ile
XM_017011107.2:c.4799C>T	XP_016866596.1:p.Thr1600Ile
XR_002956289.1:n.5094C>T
NM_001363725.2:c.2648C>T	NP_001350654.1:p.Thr883Ile
NM_001371656.1:c.5027C>T	NP_001358585.1:p.Thr1676Ile
NM_001374820.1:c.5027C>T	NP_001361749.1:p.Thr1676Ile
NM_001374828.1:c.5147C>T MANE Select	NP_001361757.1:p.Thr1716Ile
NM_017519.3:c.4988C>T	NP_059989.3:p.Thr1663Ile