Canonical Allele Identifier: CA366242639

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522475G>A (hg19) ; chr6:g.157201341G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201341G>A , CM000668.2:g.157201341G>A	GRCh38
NC_000006.11:g.157522475G>A , CM000668.1:g.157522475G>A	GRCh37
NC_000006.10:g.157564167G>A	NCBI36
NG_032093.1:g.428412G>A
NG_032093.2:g.428412G>A
NG_066624.1:g.430316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4957G>A	ENSP00000055163.8:p.Val1653Ile
ENST00000414678.8:c.5026G>A	ENSP00000412835.3:p.Val1676Ile
ENST00000637015.2:c.5245G>A	ENSP00000489729.2:p.Val1749Ile
ENST00000346085.10:c.4996G>A	ENSP00000344546.5:p.Val1666Ile
ENST00000350026.10:c.4708G>A	ENSP00000055163.7:p.Val1570Ile
ENST00000414678.7:c.3274G>A	ENSP00000412835.2:p.Val1092Ile
ENST00000635849.1:c.2437G>A	ENSP00000490948.1:p.Val813Ile
ENST00000635957.1:c.2068G>A	ENSP00000490385.1:p.Val690Ile
ENST00000636227.1:n.3579G>A
ENST00000636254.1:n.1036G>A
ENST00000636930.2:c.5116G>A MANE Select	ENSP00000490491.2:p.Val1706Ile
ENST00000636940.1:n.3113G>A
ENST00000637015.1:c.2484G>A
ENST00000637568.1:c.2398G>A
ENST00000637741.1:n.1782G>A
ENST00000637810.1:c.2458G>A	ENSP00000489636.1:p.Val820Ile
ENST00000637904.1:c.2617G>A	ENSP00000490550.1:p.Val873Ile
ENST00000647938.1:c.4747G>A	ENSP00000498155.1:p.Val1583Ile
ENST00000346085.9:c.4747G>A	ENSP00000344546.4:p.Val1583Ile
ENST00000350026.9:c.4708G>A	ENSP00000055163.7:p.Val1570Ile
ENST00000414678.6:c.3274G>A	ENSP00000412835.2:p.Val1092Ile
NM_017519.2:c.4708G>A	NP_059989.2:p.Val1570Ile
NM_020732.3:c.4747G>A	NP_065783.3:p.Val1583Ile
XM_005267069.3:c.4867G>A	XP_005267126.2:p.Val1623Ile
XM_011535984.1:c.3946G>A	XP_011534286.1:p.Val1316Ile
XM_011535985.1:c.3766G>A	XP_011534287.1:p.Val1256Ile
XM_011535986.1:c.3526G>A	XP_011534288.1:p.Val1176Ile
XM_011535987.1:c.3145G>A	XP_011534289.1:p.Val1049Ile
XM_011535988.1:c.2008G>A	XP_011534290.1:p.Val670Ile
NM_001346813.1:c.4867G>A	NP_001333742.1:p.Val1623Ile
NM_001363725.1:c.2617G>A	NP_001350654.1:p.Val873Ile
XM_011535984.2:c.5077G>A	XP_011534286.2:p.Val1693Ile
XM_011535988.3:c.2008G>A	XP_011534290.1:p.Val670Ile
XM_017011103.2:c.4978G>A	XP_016866592.1:p.Val1660Ile
XM_017011104.1:c.4948G>A	XP_016866593.1:p.Val1650Ile
XM_017011105.2:c.4918G>A	XP_016866594.1:p.Val1640Ile
XM_017011106.2:c.4789G>A	XP_016866595.1:p.Val1597Ile
XM_017011107.2:c.4768G>A	XP_016866596.1:p.Val1590Ile
XR_002956289.1:n.5063G>A
NM_001363725.2:c.2617G>A	NP_001350654.1:p.Val873Ile
NM_001371656.1:c.4996G>A	NP_001358585.1:p.Val1666Ile
NM_001374820.1:c.4996G>A	NP_001361749.1:p.Val1666Ile
NM_001374828.1:c.5116G>A MANE Select	NP_001361757.1:p.Val1706Ile
NM_017519.3:c.4957G>A	NP_059989.3:p.Val1653Ile