Canonical Allele Identifier: CA366234628

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511177G>T (hg19) ; chr6:g.157190043G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190043G>T , CM000668.2:g.157190043G>T	GRCh38
NC_000006.11:g.157511177G>T , CM000668.1:g.157511177G>T	GRCh37
NC_000006.10:g.157552869G>T	NCBI36
NG_032093.1:g.417114G>T
NG_032093.2:g.417114G>T
NG_066624.1:g.419018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3905G>T	ENSP00000055163.8:p.Ser1302Ile
ENST00000414678.8:c.3974G>T	ENSP00000412835.3:p.Ser1325Ile
ENST00000637015.2:c.4193G>T	ENSP00000489729.2:p.Ser1398Ile
ENST00000346085.10:c.3944G>T	ENSP00000344546.5:p.Ser1315Ile
ENST00000350026.10:c.3656G>T	ENSP00000055163.7:p.Ser1219Ile
ENST00000414678.7:c.2222G>T	ENSP00000412835.2:p.Ser741Ile
ENST00000635849.1:c.1385G>T	ENSP00000490948.1:p.Ser462Ile
ENST00000635957.1:c.1016G>T	ENSP00000490385.1:p.Ser339Ile
ENST00000636930.2:c.4064G>T MANE Select	ENSP00000490491.2:p.Ser1355Ile
ENST00000636940.1:n.2061G>T
ENST00000637015.1:c.1432G>T
ENST00000637568.1:c.1346G>T
ENST00000637741.1:n.730G>T
ENST00000637810.1:c.1406G>T	ENSP00000489636.1:p.Ser469Ile
ENST00000637904.1:c.1565G>T	ENSP00000490550.1:p.Ser522Ile
ENST00000647938.1:c.3695G>T	ENSP00000498155.1:p.Ser1232Ile
ENST00000346085.9:c.3695G>T	ENSP00000344546.4:p.Ser1232Ile
ENST00000350026.9:c.3656G>T	ENSP00000055163.7:p.Ser1219Ile
ENST00000414678.6:c.2222G>T	ENSP00000412835.2:p.Ser741Ile
NM_017519.2:c.3656G>T	NP_059989.2:p.Ser1219Ile
NM_020732.3:c.3695G>T	NP_065783.3:p.Ser1232Ile
XM_005267069.3:c.3815G>T	XP_005267126.2:p.Ser1272Ile
XM_011535984.1:c.2894G>T	XP_011534286.1:p.Ser965Ile
XM_011535985.1:c.2714G>T	XP_011534287.1:p.Ser905Ile
XM_011535986.1:c.2474G>T	XP_011534288.1:p.Ser825Ile
XM_011535987.1:c.2093G>T	XP_011534289.1:p.Ser698Ile
XM_011535988.1:c.956G>T	XP_011534290.1:p.Ser319Ile
NM_001346813.1:c.3815G>T	NP_001333742.1:p.Ser1272Ile
NM_001363725.1:c.1565G>T	NP_001350654.1:p.Ser522Ile
XM_011535984.2:c.4025G>T	XP_011534286.2:p.Ser1342Ile
XM_011535988.3:c.956G>T	XP_011534290.1:p.Ser319Ile
XM_017011103.2:c.3926G>T	XP_016866592.1:p.Ser1309Ile
XM_017011104.1:c.3896G>T	XP_016866593.1:p.Ser1299Ile
XM_017011105.2:c.3866G>T	XP_016866594.1:p.Ser1289Ile
XM_017011106.2:c.3737G>T	XP_016866595.1:p.Ser1246Ile
XM_017011107.2:c.3716G>T	XP_016866596.1:p.Ser1239Ile
XR_002956289.1:n.4108G>T
NM_001363725.2:c.1565G>T	NP_001350654.1:p.Ser522Ile
NM_001371656.1:c.3944G>T	NP_001358585.1:p.Ser1315Ile
NM_001374820.1:c.3944G>T	NP_001361749.1:p.Ser1315Ile
NM_001374828.1:c.4064G>T MANE Select	NP_001361757.1:p.Ser1355Ile
NM_017519.3:c.3905G>T	NP_059989.3:p.Ser1302Ile