Canonical Allele Identifier: CA150368542

Gene: ARID1B

Linked Data

• dbSNP Id: rs565147002
• gnomAD v3: 6-157198814-T-G
• gnomAD v4: 6-157198814-T-G
• MyVariant Identifiers: chr6:g.157519948T>G (hg19) ; chr6:g.157198814T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198814T>G , CM000668.2:g.157198814T>G	GRCh38
NC_000006.11:g.157519948T>G , CM000668.1:g.157519948T>G	GRCh37
NC_000006.10:g.157561640T>G	NCBI36
NG_032093.1:g.425885T>G
NG_032093.2:g.425885T>G
NG_066624.1:g.427789T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4227T>G	ENSP00000055163.8:p.His1409Gln
ENST00000414678.8:c.4296T>G	ENSP00000412835.3:p.His1432Gln
ENST00000637015.2:c.4515T>G	ENSP00000489729.2:p.His1505Gln
ENST00000346085.10:c.4266T>G	ENSP00000344546.5:p.His1422Gln
ENST00000350026.10:c.3978T>G	ENSP00000055163.7:p.His1326Gln
ENST00000414678.7:c.2544T>G	ENSP00000412835.2:p.His848Gln
ENST00000635849.1:c.1707T>G	ENSP00000490948.1:p.His569Gln
ENST00000635957.1:c.1338T>G	ENSP00000490385.1:p.His446Gln
ENST00000636227.1:n.2849T>G
ENST00000636254.1:n.306T>G
ENST00000636930.2:c.4386T>G MANE Select	ENSP00000490491.2:p.His1462Gln
ENST00000636940.1:n.2383T>G
ENST00000637015.1:c.1754T>G
ENST00000637568.1:c.1668T>G
ENST00000637741.1:n.1052T>G
ENST00000637810.1:c.1728T>G	ENSP00000489636.1:p.His576Gln
ENST00000637904.1:c.1887T>G	ENSP00000490550.1:p.His629Gln
ENST00000647938.1:c.4017T>G	ENSP00000498155.1:p.His1339Gln
ENST00000346085.9:c.4017T>G	ENSP00000344546.4:p.His1339Gln
ENST00000350026.9:c.3978T>G	ENSP00000055163.7:p.His1326Gln
ENST00000414678.6:c.2544T>G	ENSP00000412835.2:p.His848Gln
NM_017519.2:c.3978T>G	NP_059989.2:p.His1326Gln
NM_020732.3:c.4017T>G	NP_065783.3:p.His1339Gln
XM_005267069.3:c.4137T>G	XP_005267126.2:p.His1379Gln
XM_011535984.1:c.3216T>G	XP_011534286.1:p.His1072Gln
XM_011535985.1:c.3036T>G	XP_011534287.1:p.His1012Gln
XM_011535986.1:c.2796T>G	XP_011534288.1:p.His932Gln
XM_011535987.1:c.2415T>G	XP_011534289.1:p.His805Gln
XM_011535988.1:c.1278T>G	XP_011534290.1:p.His426Gln
NM_001346813.1:c.4137T>G	NP_001333742.1:p.His1379Gln
NM_001363725.1:c.1887T>G	NP_001350654.1:p.His629Gln
XM_011535984.2:c.4347T>G	XP_011534286.2:p.His1449Gln
XM_011535988.3:c.1278T>G	XP_011534290.1:p.His426Gln
XM_017011103.2:c.4248T>G	XP_016866592.1:p.His1416Gln
XM_017011104.1:c.4218T>G	XP_016866593.1:p.His1406Gln
XM_017011105.2:c.4188T>G	XP_016866594.1:p.His1396Gln
XM_017011106.2:c.4059T>G	XP_016866595.1:p.His1353Gln
XM_017011107.2:c.4038T>G	XP_016866596.1:p.His1346Gln
XR_002956289.1:n.4427-1891T>G
NM_001363725.2:c.1887T>G	NP_001350654.1:p.His629Gln
NM_001371656.1:c.4266T>G	NP_001358585.1:p.His1422Gln
NM_001374820.1:c.4266T>G	NP_001361749.1:p.His1422Gln
NM_001374828.1:c.4386T>G MANE Select	NP_001361757.1:p.His1462Gln
NM_017519.3:c.4227T>G	NP_059989.3:p.His1409Gln