Canonical Allele Identifier: CA366234135

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3827T>C	ENSP00000055163.8:p.Val1276Ala
ENST00000414678.8:c.3896T>C	ENSP00000412835.3:p.Val1299Ala
ENST00000637015.2:c.4115T>C	ENSP00000489729.2:p.Val1372Ala
ENST00000346085.10:c.3866T>C	ENSP00000344546.5:p.Val1289Ala
ENST00000350026.10:c.3578T>C	ENSP00000055163.7:p.Val1193Ala
ENST00000414678.7:c.2144T>C	ENSP00000412835.2:p.Val715Ala
ENST00000635849.1:c.1307T>C	ENSP00000490948.1:p.Val436Ala
ENST00000635957.1:c.941T>C	ENSP00000490385.1:p.Val314Ala
ENST00000636930.2:c.3986T>C MANE Select	ENSP00000490491.2:p.Val1329Ala
ENST00000636940.1:n.1983T>C
ENST00000637015.1:c.1354T>C
ENST00000637568.1:c.1268T>C
ENST00000637741.1:n.652T>C
ENST00000637810.1:c.1328T>C	ENSP00000489636.1:p.Val443Ala
ENST00000637904.1:c.1487T>C	ENSP00000490550.1:p.Val496Ala
ENST00000647938.1:c.3617T>C	ENSP00000498155.1:p.Val1206Ala
ENST00000346085.9:c.3617T>C	ENSP00000344546.4:p.Val1206Ala
ENST00000350026.9:c.3578T>C	ENSP00000055163.7:p.Val1193Ala
ENST00000414678.6:c.2144T>C	ENSP00000412835.2:p.Val715Ala
NM_017519.2:c.3578T>C	NP_059989.2:p.Val1193Ala
NM_020732.3:c.3617T>C	NP_065783.3:p.Val1206Ala
XM_005267069.3:c.3737T>C	XP_005267126.2:p.Val1246Ala
XM_011535984.1:c.2816T>C	XP_011534286.1:p.Val939Ala
XM_011535985.1:c.2636T>C	XP_011534287.1:p.Val879Ala
XM_011535986.1:c.2396T>C	XP_011534288.1:p.Val799Ala
XM_011535987.1:c.2015T>C	XP_011534289.1:p.Val672Ala
XM_011535988.1:c.878T>C	XP_011534290.1:p.Val293Ala
NM_001346813.1:c.3737T>C	NP_001333742.1:p.Val1246Ala
NM_001363725.1:c.1487T>C	NP_001350654.1:p.Val496Ala
XM_011535984.2:c.3947T>C	XP_011534286.2:p.Val1316Ala
XM_011535988.3:c.878T>C	XP_011534290.1:p.Val293Ala
XM_017011103.2:c.3848T>C	XP_016866592.1:p.Val1283Ala
XM_017011104.1:c.3818T>C	XP_016866593.1:p.Val1273Ala
XM_017011105.2:c.3788T>C	XP_016866594.1:p.Val1263Ala
XM_017011106.2:c.3659T>C	XP_016866595.1:p.Val1220Ala
XM_017011107.2:c.3638T>C	XP_016866596.1:p.Val1213Ala
XR_002956289.1:n.4030T>C
NM_001363725.2:c.1487T>C	NP_001350654.1:p.Val496Ala
NM_001371656.1:c.3866T>C	NP_001358585.1:p.Val1289Ala
NM_001374820.1:c.3866T>C	NP_001361749.1:p.Val1289Ala
NM_001374828.1:c.3986T>C MANE Select	NP_001361757.1:p.Val1329Ala
NM_017519.3:c.3827T>C	NP_059989.3:p.Val1276Ala