Canonical Allele Identifier: CA366234147

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510848G>T (hg19) ; chr6:g.157189714G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189714G>T , CM000668.2:g.157189714G>T	GRCh38
NC_000006.11:g.157510848G>T , CM000668.1:g.157510848G>T	GRCh37
NC_000006.10:g.157552540G>T	NCBI36
NG_032093.1:g.416785G>T
NG_032093.2:g.416785G>T
NG_066624.1:g.418689G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3833G>T	ENSP00000055163.8:p.Gly1278Val
ENST00000414678.8:c.3902G>T	ENSP00000412835.3:p.Gly1301Val
ENST00000637015.2:c.4121G>T	ENSP00000489729.2:p.Gly1374Val
ENST00000346085.10:c.3872G>T	ENSP00000344546.5:p.Gly1291Val
ENST00000350026.10:c.3584G>T	ENSP00000055163.7:p.Gly1195Val
ENST00000414678.7:c.2150G>T	ENSP00000412835.2:p.Gly717Val
ENST00000635849.1:c.1313G>T	ENSP00000490948.1:p.Gly438Val
ENST00000635957.1:c.947G>T	ENSP00000490385.1:p.Gly316Val
ENST00000636930.2:c.3992G>T MANE Select	ENSP00000490491.2:p.Gly1331Val
ENST00000636940.1:n.1989G>T
ENST00000637015.1:c.1360G>T
ENST00000637568.1:c.1274G>T
ENST00000637741.1:n.658G>T
ENST00000637810.1:c.1334G>T	ENSP00000489636.1:p.Gly445Val
ENST00000637904.1:c.1493G>T	ENSP00000490550.1:p.Gly498Val
ENST00000647938.1:c.3623G>T	ENSP00000498155.1:p.Gly1208Val
ENST00000346085.9:c.3623G>T	ENSP00000344546.4:p.Gly1208Val
ENST00000350026.9:c.3584G>T	ENSP00000055163.7:p.Gly1195Val
ENST00000414678.6:c.2150G>T	ENSP00000412835.2:p.Gly717Val
NM_017519.2:c.3584G>T	NP_059989.2:p.Gly1195Val
NM_020732.3:c.3623G>T	NP_065783.3:p.Gly1208Val
XM_005267069.3:c.3743G>T	XP_005267126.2:p.Gly1248Val
XM_011535984.1:c.2822G>T	XP_011534286.1:p.Gly941Val
XM_011535985.1:c.2642G>T	XP_011534287.1:p.Gly881Val
XM_011535986.1:c.2402G>T	XP_011534288.1:p.Gly801Val
XM_011535987.1:c.2021G>T	XP_011534289.1:p.Gly674Val
XM_011535988.1:c.884G>T	XP_011534290.1:p.Gly295Val
NM_001346813.1:c.3743G>T	NP_001333742.1:p.Gly1248Val
NM_001363725.1:c.1493G>T	NP_001350654.1:p.Gly498Val
XM_011535984.2:c.3953G>T	XP_011534286.2:p.Gly1318Val
XM_011535988.3:c.884G>T	XP_011534290.1:p.Gly295Val
XM_017011103.2:c.3854G>T	XP_016866592.1:p.Gly1285Val
XM_017011104.1:c.3824G>T	XP_016866593.1:p.Gly1275Val
XM_017011105.2:c.3794G>T	XP_016866594.1:p.Gly1265Val
XM_017011106.2:c.3665G>T	XP_016866595.1:p.Gly1222Val
XM_017011107.2:c.3644G>T	XP_016866596.1:p.Gly1215Val
XR_002956289.1:n.4036G>T
NM_001363725.2:c.1493G>T	NP_001350654.1:p.Gly498Val
NM_001371656.1:c.3872G>T	NP_001358585.1:p.Gly1291Val
NM_001374820.1:c.3872G>T	NP_001361749.1:p.Gly1291Val
NM_001374828.1:c.3992G>T MANE Select	NP_001361757.1:p.Gly1331Val
NM_017519.3:c.3833G>T	NP_059989.3:p.Gly1278Val