Canonical Allele Identifier: CA150368555

Gene: ARID1B

Linked Data

• dbSNP Id: rs1011344782
• gnomAD v4: 6-157198861-A-G
• MyVariant Identifiers: chr6:g.157519995A>G (hg19) ; chr6:g.157198861A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198861A>G , CM000668.2:g.157198861A>G	GRCh38
NC_000006.11:g.157519995A>G , CM000668.1:g.157519995A>G	GRCh37
NC_000006.10:g.157561687A>G	NCBI36
NG_032093.1:g.425932A>G
NG_032093.2:g.425932A>G
NG_066624.1:g.427836A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4274A>G	ENSP00000055163.8:p.Gln1425Arg
ENST00000414678.8:c.4343A>G	ENSP00000412835.3:p.Gln1448Arg
ENST00000637015.2:c.4562A>G	ENSP00000489729.2:p.Gln1521Arg
ENST00000346085.10:c.4313A>G	ENSP00000344546.5:p.Gln1438Arg
ENST00000350026.10:c.4025A>G	ENSP00000055163.7:p.Gln1342Arg
ENST00000414678.7:c.2591A>G	ENSP00000412835.2:p.Gln864Arg
ENST00000635849.1:c.1754A>G	ENSP00000490948.1:p.Gln585Arg
ENST00000635957.1:c.1385A>G	ENSP00000490385.1:p.Gln462Arg
ENST00000636227.1:n.2896A>G
ENST00000636254.1:n.353A>G
ENST00000636930.2:c.4433A>G MANE Select	ENSP00000490491.2:p.Gln1478Arg
ENST00000636940.1:n.2430A>G
ENST00000637015.1:c.1801A>G
ENST00000637568.1:c.1715A>G
ENST00000637741.1:n.1099A>G
ENST00000637810.1:c.1775A>G	ENSP00000489636.1:p.Gln592Arg
ENST00000637904.1:c.1934A>G	ENSP00000490550.1:p.Gln645Arg
ENST00000647938.1:c.4064A>G	ENSP00000498155.1:p.Gln1355Arg
ENST00000346085.9:c.4064A>G	ENSP00000344546.4:p.Gln1355Arg
ENST00000350026.9:c.4025A>G	ENSP00000055163.7:p.Gln1342Arg
ENST00000414678.6:c.2591A>G	ENSP00000412835.2:p.Gln864Arg
NM_017519.2:c.4025A>G	NP_059989.2:p.Gln1342Arg
NM_020732.3:c.4064A>G	NP_065783.3:p.Gln1355Arg
XM_005267069.3:c.4184A>G	XP_005267126.2:p.Gln1395Arg
XM_011535984.1:c.3263A>G	XP_011534286.1:p.Gln1088Arg
XM_011535985.1:c.3083A>G	XP_011534287.1:p.Gln1028Arg
XM_011535986.1:c.2843A>G	XP_011534288.1:p.Gln948Arg
XM_011535987.1:c.2462A>G	XP_011534289.1:p.Gln821Arg
XM_011535988.1:c.1325A>G	XP_011534290.1:p.Gln442Arg
NM_001346813.1:c.4184A>G	NP_001333742.1:p.Gln1395Arg
NM_001363725.1:c.1934A>G	NP_001350654.1:p.Gln645Arg
XM_011535984.2:c.4394A>G	XP_011534286.2:p.Gln1465Arg
XM_011535988.3:c.1325A>G	XP_011534290.1:p.Gln442Arg
XM_017011103.2:c.4295A>G	XP_016866592.1:p.Gln1432Arg
XM_017011104.1:c.4265A>G	XP_016866593.1:p.Gln1422Arg
XM_017011105.2:c.4235A>G	XP_016866594.1:p.Gln1412Arg
XM_017011106.2:c.4106A>G	XP_016866595.1:p.Gln1369Arg
XM_017011107.2:c.4085A>G	XP_016866596.1:p.Gln1362Arg
XR_002956289.1:n.4427-1844A>G
NM_001363725.2:c.1934A>G	NP_001350654.1:p.Gln645Arg
NM_001371656.1:c.4313A>G	NP_001358585.1:p.Gln1438Arg
NM_001374820.1:c.4313A>G	NP_001361749.1:p.Gln1438Arg
NM_001374828.1:c.4433A>G MANE Select	NP_001361757.1:p.Gln1478Arg
NM_017519.3:c.4274A>G	NP_059989.3:p.Gln1425Arg