Canonical Allele Identifier: CA366234136

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510842T>G (hg19) ; chr6:g.157189708T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189708T>G , CM000668.2:g.157189708T>G	GRCh38
NC_000006.11:g.157510842T>G , CM000668.1:g.157510842T>G	GRCh37
NC_000006.10:g.157552534T>G	NCBI36
NG_032093.1:g.416779T>G
NG_032093.2:g.416779T>G
NG_066624.1:g.418683T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3827T>G	ENSP00000055163.8:p.Val1276Gly
ENST00000414678.8:c.3896T>G	ENSP00000412835.3:p.Val1299Gly
ENST00000637015.2:c.4115T>G	ENSP00000489729.2:p.Val1372Gly
ENST00000346085.10:c.3866T>G	ENSP00000344546.5:p.Val1289Gly
ENST00000350026.10:c.3578T>G	ENSP00000055163.7:p.Val1193Gly
ENST00000414678.7:c.2144T>G	ENSP00000412835.2:p.Val715Gly
ENST00000635849.1:c.1307T>G	ENSP00000490948.1:p.Val436Gly
ENST00000635957.1:c.941T>G	ENSP00000490385.1:p.Val314Gly
ENST00000636930.2:c.3986T>G MANE Select	ENSP00000490491.2:p.Val1329Gly
ENST00000636940.1:n.1983T>G
ENST00000637015.1:c.1354T>G
ENST00000637568.1:c.1268T>G
ENST00000637741.1:n.652T>G
ENST00000637810.1:c.1328T>G	ENSP00000489636.1:p.Val443Gly
ENST00000637904.1:c.1487T>G	ENSP00000490550.1:p.Val496Gly
ENST00000647938.1:c.3617T>G	ENSP00000498155.1:p.Val1206Gly
ENST00000346085.9:c.3617T>G	ENSP00000344546.4:p.Val1206Gly
ENST00000350026.9:c.3578T>G	ENSP00000055163.7:p.Val1193Gly
ENST00000414678.6:c.2144T>G	ENSP00000412835.2:p.Val715Gly
NM_017519.2:c.3578T>G	NP_059989.2:p.Val1193Gly
NM_020732.3:c.3617T>G	NP_065783.3:p.Val1206Gly
XM_005267069.3:c.3737T>G	XP_005267126.2:p.Val1246Gly
XM_011535984.1:c.2816T>G	XP_011534286.1:p.Val939Gly
XM_011535985.1:c.2636T>G	XP_011534287.1:p.Val879Gly
XM_011535986.1:c.2396T>G	XP_011534288.1:p.Val799Gly
XM_011535987.1:c.2015T>G	XP_011534289.1:p.Val672Gly
XM_011535988.1:c.878T>G	XP_011534290.1:p.Val293Gly
NM_001346813.1:c.3737T>G	NP_001333742.1:p.Val1246Gly
NM_001363725.1:c.1487T>G	NP_001350654.1:p.Val496Gly
XM_011535984.2:c.3947T>G	XP_011534286.2:p.Val1316Gly
XM_011535988.3:c.878T>G	XP_011534290.1:p.Val293Gly
XM_017011103.2:c.3848T>G	XP_016866592.1:p.Val1283Gly
XM_017011104.1:c.3818T>G	XP_016866593.1:p.Val1273Gly
XM_017011105.2:c.3788T>G	XP_016866594.1:p.Val1263Gly
XM_017011106.2:c.3659T>G	XP_016866595.1:p.Val1220Gly
XM_017011107.2:c.3638T>G	XP_016866596.1:p.Val1213Gly
XR_002956289.1:n.4030T>G
NM_001363725.2:c.1487T>G	NP_001350654.1:p.Val496Gly
NM_001371656.1:c.3866T>G	NP_001358585.1:p.Val1289Gly
NM_001374820.1:c.3866T>G	NP_001361749.1:p.Val1289Gly
NM_001374828.1:c.3986T>G MANE Select	NP_001361757.1:p.Val1329Gly
NM_017519.3:c.3827T>G	NP_059989.3:p.Val1276Gly