Canonical Allele Identifier: CA366234133

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510841G>T (hg19) ; chr6:g.157189707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189707G>T , CM000668.2:g.157189707G>T	GRCh38
NC_000006.11:g.157510841G>T , CM000668.1:g.157510841G>T	GRCh37
NC_000006.10:g.157552533G>T	NCBI36
NG_032093.1:g.416778G>T
NG_032093.2:g.416778G>T
NG_066624.1:g.418682G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3826G>T	ENSP00000055163.8:p.Val1276Phe
ENST00000414678.8:c.3895G>T	ENSP00000412835.3:p.Val1299Phe
ENST00000637015.2:c.4114G>T	ENSP00000489729.2:p.Val1372Phe
ENST00000346085.10:c.3865G>T	ENSP00000344546.5:p.Val1289Phe
ENST00000350026.10:c.3577G>T	ENSP00000055163.7:p.Val1193Phe
ENST00000414678.7:c.2143G>T	ENSP00000412835.2:p.Val715Phe
ENST00000635849.1:c.1306G>T	ENSP00000490948.1:p.Val436Phe
ENST00000635957.1:c.940G>T	ENSP00000490385.1:p.Val314Phe
ENST00000636930.2:c.3985G>T MANE Select	ENSP00000490491.2:p.Val1329Phe
ENST00000636940.1:n.1982G>T
ENST00000637015.1:c.1353G>T
ENST00000637568.1:c.1267G>T
ENST00000637741.1:n.651G>T
ENST00000637810.1:c.1327G>T	ENSP00000489636.1:p.Val443Phe
ENST00000637904.1:c.1486G>T	ENSP00000490550.1:p.Val496Phe
ENST00000647938.1:c.3616G>T	ENSP00000498155.1:p.Val1206Phe
ENST00000346085.9:c.3616G>T	ENSP00000344546.4:p.Val1206Phe
ENST00000350026.9:c.3577G>T	ENSP00000055163.7:p.Val1193Phe
ENST00000414678.6:c.2143G>T	ENSP00000412835.2:p.Val715Phe
NM_017519.2:c.3577G>T	NP_059989.2:p.Val1193Phe
NM_020732.3:c.3616G>T	NP_065783.3:p.Val1206Phe
XM_005267069.3:c.3736G>T	XP_005267126.2:p.Val1246Phe
XM_011535984.1:c.2815G>T	XP_011534286.1:p.Val939Phe
XM_011535985.1:c.2635G>T	XP_011534287.1:p.Val879Phe
XM_011535986.1:c.2395G>T	XP_011534288.1:p.Val799Phe
XM_011535987.1:c.2014G>T	XP_011534289.1:p.Val672Phe
XM_011535988.1:c.877G>T	XP_011534290.1:p.Val293Phe
NM_001346813.1:c.3736G>T	NP_001333742.1:p.Val1246Phe
NM_001363725.1:c.1486G>T	NP_001350654.1:p.Val496Phe
XM_011535984.2:c.3946G>T	XP_011534286.2:p.Val1316Phe
XM_011535988.3:c.877G>T	XP_011534290.1:p.Val293Phe
XM_017011103.2:c.3847G>T	XP_016866592.1:p.Val1283Phe
XM_017011104.1:c.3817G>T	XP_016866593.1:p.Val1273Phe
XM_017011105.2:c.3787G>T	XP_016866594.1:p.Val1263Phe
XM_017011106.2:c.3658G>T	XP_016866595.1:p.Val1220Phe
XM_017011107.2:c.3637G>T	XP_016866596.1:p.Val1213Phe
XR_002956289.1:n.4029G>T
NM_001363725.2:c.1486G>T	NP_001350654.1:p.Val496Phe
NM_001371656.1:c.3865G>T	NP_001358585.1:p.Val1289Phe
NM_001374820.1:c.3865G>T	NP_001361749.1:p.Val1289Phe
NM_001374828.1:c.3985G>T MANE Select	NP_001361757.1:p.Val1329Phe
NM_017519.3:c.3826G>T	NP_059989.3:p.Val1276Phe