Canonical Allele Identifier: CA366234609

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2531161
• ClinVar RCV Id: RCV003246433
• MyVariant Identifiers: chr6:g.157511176A>G (hg19) ; chr6:g.157190042A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190042A>G , CM000668.2:g.157190042A>G	GRCh38
NC_000006.11:g.157511176A>G , CM000668.1:g.157511176A>G	GRCh37
NC_000006.10:g.157552868A>G	NCBI36
NG_032093.1:g.417113A>G
NG_032093.2:g.417113A>G
NG_066624.1:g.419017A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3904A>G	ENSP00000055163.8:p.Ser1302Gly
ENST00000414678.8:c.3973A>G	ENSP00000412835.3:p.Ser1325Gly
ENST00000637015.2:c.4192A>G	ENSP00000489729.2:p.Ser1398Gly
ENST00000346085.10:c.3943A>G	ENSP00000344546.5:p.Ser1315Gly
ENST00000350026.10:c.3655A>G	ENSP00000055163.7:p.Ser1219Gly
ENST00000414678.7:c.2221A>G	ENSP00000412835.2:p.Ser741Gly
ENST00000635849.1:c.1384A>G	ENSP00000490948.1:p.Ser462Gly
ENST00000635957.1:c.1015A>G	ENSP00000490385.1:p.Ser339Gly
ENST00000636930.2:c.4063A>G MANE Select	ENSP00000490491.2:p.Ser1355Gly
ENST00000636940.1:n.2060A>G
ENST00000637015.1:c.1431A>G
ENST00000637568.1:c.1345A>G
ENST00000637741.1:n.729A>G
ENST00000637810.1:c.1405A>G	ENSP00000489636.1:p.Ser469Gly
ENST00000637904.1:c.1564A>G	ENSP00000490550.1:p.Ser522Gly
ENST00000647938.1:c.3694A>G	ENSP00000498155.1:p.Ser1232Gly
ENST00000346085.9:c.3694A>G	ENSP00000344546.4:p.Ser1232Gly
ENST00000350026.9:c.3655A>G	ENSP00000055163.7:p.Ser1219Gly
ENST00000414678.6:c.2221A>G	ENSP00000412835.2:p.Ser741Gly
NM_017519.2:c.3655A>G	NP_059989.2:p.Ser1219Gly
NM_020732.3:c.3694A>G	NP_065783.3:p.Ser1232Gly
XM_005267069.3:c.3814A>G	XP_005267126.2:p.Ser1272Gly
XM_011535984.1:c.2893A>G	XP_011534286.1:p.Ser965Gly
XM_011535985.1:c.2713A>G	XP_011534287.1:p.Ser905Gly
XM_011535986.1:c.2473A>G	XP_011534288.1:p.Ser825Gly
XM_011535987.1:c.2092A>G	XP_011534289.1:p.Ser698Gly
XM_011535988.1:c.955A>G	XP_011534290.1:p.Ser319Gly
NM_001346813.1:c.3814A>G	NP_001333742.1:p.Ser1272Gly
NM_001363725.1:c.1564A>G	NP_001350654.1:p.Ser522Gly
XM_011535984.2:c.4024A>G	XP_011534286.2:p.Ser1342Gly
XM_011535988.3:c.955A>G	XP_011534290.1:p.Ser319Gly
XM_017011103.2:c.3925A>G	XP_016866592.1:p.Ser1309Gly
XM_017011104.1:c.3895A>G	XP_016866593.1:p.Ser1299Gly
XM_017011105.2:c.3865A>G	XP_016866594.1:p.Ser1289Gly
XM_017011106.2:c.3736A>G	XP_016866595.1:p.Ser1246Gly
XM_017011107.2:c.3715A>G	XP_016866596.1:p.Ser1239Gly
XR_002956289.1:n.4107A>G
NM_001363725.2:c.1564A>G	NP_001350654.1:p.Ser522Gly
NM_001371656.1:c.3943A>G	NP_001358585.1:p.Ser1315Gly
NM_001374820.1:c.3943A>G	NP_001361749.1:p.Ser1315Gly
NM_001374828.1:c.4063A>G MANE Select	NP_001361757.1:p.Ser1355Gly
NM_017519.3:c.3904A>G	NP_059989.3:p.Ser1302Gly