Canonical Allele Identifier: CA366234618

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3905G>A	ENSP00000055163.8:p.Ser1302Asn
ENST00000414678.8:c.3974G>A	ENSP00000412835.3:p.Ser1325Asn
ENST00000637015.2:c.4193G>A	ENSP00000489729.2:p.Ser1398Asn
ENST00000346085.10:c.3944G>A	ENSP00000344546.5:p.Ser1315Asn
ENST00000350026.10:c.3656G>A	ENSP00000055163.7:p.Ser1219Asn
ENST00000414678.7:c.2222G>A	ENSP00000412835.2:p.Ser741Asn
ENST00000635849.1:c.1385G>A	ENSP00000490948.1:p.Ser462Asn
ENST00000635957.1:c.1016G>A	ENSP00000490385.1:p.Ser339Asn
ENST00000636930.2:c.4064G>A MANE Select	ENSP00000490491.2:p.Ser1355Asn
ENST00000636940.1:n.2061G>A
ENST00000637015.1:c.1432G>A
ENST00000637568.1:c.1346G>A
ENST00000637741.1:n.730G>A
ENST00000637810.1:c.1406G>A	ENSP00000489636.1:p.Ser469Asn
ENST00000637904.1:c.1565G>A	ENSP00000490550.1:p.Ser522Asn
ENST00000647938.1:c.3695G>A	ENSP00000498155.1:p.Ser1232Asn
ENST00000346085.9:c.3695G>A	ENSP00000344546.4:p.Ser1232Asn
ENST00000350026.9:c.3656G>A	ENSP00000055163.7:p.Ser1219Asn
ENST00000414678.6:c.2222G>A	ENSP00000412835.2:p.Ser741Asn
NM_017519.2:c.3656G>A	NP_059989.2:p.Ser1219Asn
NM_020732.3:c.3695G>A	NP_065783.3:p.Ser1232Asn
XM_005267069.3:c.3815G>A	XP_005267126.2:p.Ser1272Asn
XM_011535984.1:c.2894G>A	XP_011534286.1:p.Ser965Asn
XM_011535985.1:c.2714G>A	XP_011534287.1:p.Ser905Asn
XM_011535986.1:c.2474G>A	XP_011534288.1:p.Ser825Asn
XM_011535987.1:c.2093G>A	XP_011534289.1:p.Ser698Asn
XM_011535988.1:c.956G>A	XP_011534290.1:p.Ser319Asn
NM_001346813.1:c.3815G>A	NP_001333742.1:p.Ser1272Asn
NM_001363725.1:c.1565G>A	NP_001350654.1:p.Ser522Asn
XM_011535984.2:c.4025G>A	XP_011534286.2:p.Ser1342Asn
XM_011535988.3:c.956G>A	XP_011534290.1:p.Ser319Asn
XM_017011103.2:c.3926G>A	XP_016866592.1:p.Ser1309Asn
XM_017011104.1:c.3896G>A	XP_016866593.1:p.Ser1299Asn
XM_017011105.2:c.3866G>A	XP_016866594.1:p.Ser1289Asn
XM_017011106.2:c.3737G>A	XP_016866595.1:p.Ser1246Asn
XM_017011107.2:c.3716G>A	XP_016866596.1:p.Ser1239Asn
XR_002956289.1:n.4108G>A
NM_001363725.2:c.1565G>A	NP_001350654.1:p.Ser522Asn
NM_001371656.1:c.3944G>A	NP_001358585.1:p.Ser1315Asn
NM_001374820.1:c.3944G>A	NP_001361749.1:p.Ser1315Asn
NM_001374828.1:c.4064G>A MANE Select	NP_001361757.1:p.Ser1355Asn
NM_017519.3:c.3905G>A	NP_059989.3:p.Ser1302Asn