Canonical Allele Identifier: CA366239444

Gene: ARID1B

Linked Data

• dbSNP Id: rs1301271574
• gnomAD v2: 6-157519947-A-G
• gnomAD v3: 6-157198813-A-G
• gnomAD v4: 6-157198813-A-G
• MyVariant Identifiers: chr6:g.157519947A>G (hg19) ; chr6:g.157198813A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198813A>G , CM000668.2:g.157198813A>G	GRCh38
NC_000006.11:g.157519947A>G , CM000668.1:g.157519947A>G	GRCh37
NC_000006.10:g.157561639A>G	NCBI36
NG_032093.1:g.425884A>G
NG_032093.2:g.425884A>G
NG_066624.1:g.427788A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4226A>G	ENSP00000055163.8:p.His1409Arg
ENST00000414678.8:c.4295A>G	ENSP00000412835.3:p.His1432Arg
ENST00000637015.2:c.4514A>G	ENSP00000489729.2:p.His1505Arg
ENST00000346085.10:c.4265A>G	ENSP00000344546.5:p.His1422Arg
ENST00000350026.10:c.3977A>G	ENSP00000055163.7:p.His1326Arg
ENST00000414678.7:c.2543A>G	ENSP00000412835.2:p.His848Arg
ENST00000635849.1:c.1706A>G	ENSP00000490948.1:p.His569Arg
ENST00000635957.1:c.1337A>G	ENSP00000490385.1:p.His446Arg
ENST00000636227.1:n.2848A>G
ENST00000636254.1:n.305A>G
ENST00000636930.2:c.4385A>G MANE Select	ENSP00000490491.2:p.His1462Arg
ENST00000636940.1:n.2382A>G
ENST00000637015.1:c.1753A>G
ENST00000637568.1:c.1667A>G
ENST00000637741.1:n.1051A>G
ENST00000637810.1:c.1727A>G	ENSP00000489636.1:p.His576Arg
ENST00000637904.1:c.1886A>G	ENSP00000490550.1:p.His629Arg
ENST00000647938.1:c.4016A>G	ENSP00000498155.1:p.His1339Arg
ENST00000346085.9:c.4016A>G	ENSP00000344546.4:p.His1339Arg
ENST00000350026.9:c.3977A>G	ENSP00000055163.7:p.His1326Arg
ENST00000414678.6:c.2543A>G	ENSP00000412835.2:p.His848Arg
NM_017519.2:c.3977A>G	NP_059989.2:p.His1326Arg
NM_020732.3:c.4016A>G	NP_065783.3:p.His1339Arg
XM_005267069.3:c.4136A>G	XP_005267126.2:p.His1379Arg
XM_011535984.1:c.3215A>G	XP_011534286.1:p.His1072Arg
XM_011535985.1:c.3035A>G	XP_011534287.1:p.His1012Arg
XM_011535986.1:c.2795A>G	XP_011534288.1:p.His932Arg
XM_011535987.1:c.2414A>G	XP_011534289.1:p.His805Arg
XM_011535988.1:c.1277A>G	XP_011534290.1:p.His426Arg
NM_001346813.1:c.4136A>G	NP_001333742.1:p.His1379Arg
NM_001363725.1:c.1886A>G	NP_001350654.1:p.His629Arg
XM_011535984.2:c.4346A>G	XP_011534286.2:p.His1449Arg
XM_011535988.3:c.1277A>G	XP_011534290.1:p.His426Arg
XM_017011103.2:c.4247A>G	XP_016866592.1:p.His1416Arg
XM_017011104.1:c.4217A>G	XP_016866593.1:p.His1406Arg
XM_017011105.2:c.4187A>G	XP_016866594.1:p.His1396Arg
XM_017011106.2:c.4058A>G	XP_016866595.1:p.His1353Arg
XM_017011107.2:c.4037A>G	XP_016866596.1:p.His1346Arg
XR_002956289.1:n.4427-1892A>G
NM_001363725.2:c.1886A>G	NP_001350654.1:p.His629Arg
NM_001371656.1:c.4265A>G	NP_001358585.1:p.His1422Arg
NM_001374820.1:c.4265A>G	NP_001361749.1:p.His1422Arg
NM_001374828.1:c.4385A>G MANE Select	NP_001361757.1:p.His1462Arg
NM_017519.3:c.4226A>G	NP_059989.3:p.His1409Arg