Canonical Allele Identifier: CA366242952

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201404-A-G
• MyVariant Identifiers: chr6:g.157522538A>G (hg19) ; chr6:g.157201404A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201404A>G , CM000668.2:g.157201404A>G	GRCh38
NC_000006.11:g.157522538A>G , CM000668.1:g.157522538A>G	GRCh37
NC_000006.10:g.157564230A>G	NCBI36
NG_032093.1:g.428475A>G
NG_032093.2:g.428475A>G
NG_066624.1:g.430379A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5020A>G	ENSP00000055163.8:p.Arg1674Gly
ENST00000414678.8:c.5089A>G	ENSP00000412835.3:p.Arg1697Gly
ENST00000637015.2:c.5308A>G	ENSP00000489729.2:p.Arg1770Gly
ENST00000346085.10:c.5059A>G	ENSP00000344546.5:p.Arg1687Gly
ENST00000350026.10:c.4771A>G	ENSP00000055163.7:p.Arg1591Gly
ENST00000414678.7:c.3337A>G	ENSP00000412835.2:p.Arg1113Gly
ENST00000635849.1:c.2500A>G	ENSP00000490948.1:p.Arg834Gly
ENST00000635957.1:c.2131A>G	ENSP00000490385.1:p.Arg711Gly
ENST00000636227.1:n.3642A>G
ENST00000636254.1:n.1099A>G
ENST00000636930.2:c.5179A>G MANE Select	ENSP00000490491.2:p.Arg1727Gly
ENST00000636940.1:n.3176A>G
ENST00000637015.1:c.2547A>G
ENST00000637568.1:c.2461A>G
ENST00000637741.1:n.1845A>G
ENST00000637810.1:c.2521A>G	ENSP00000489636.1:p.Arg841Gly
ENST00000637904.1:c.2680A>G	ENSP00000490550.1:p.Arg894Gly
ENST00000647938.1:c.4810A>G	ENSP00000498155.1:p.Arg1604Gly
ENST00000346085.9:c.4810A>G	ENSP00000344546.4:p.Arg1604Gly
ENST00000350026.9:c.4771A>G	ENSP00000055163.7:p.Arg1591Gly
ENST00000414678.6:c.3337A>G	ENSP00000412835.2:p.Arg1113Gly
NM_017519.2:c.4771A>G	NP_059989.2:p.Arg1591Gly
NM_020732.3:c.4810A>G	NP_065783.3:p.Arg1604Gly
XM_005267069.3:c.4930A>G	XP_005267126.2:p.Arg1644Gly
XM_011535984.1:c.4009A>G	XP_011534286.1:p.Arg1337Gly
XM_011535985.1:c.3829A>G	XP_011534287.1:p.Arg1277Gly
XM_011535986.1:c.3589A>G	XP_011534288.1:p.Arg1197Gly
XM_011535987.1:c.3208A>G	XP_011534289.1:p.Arg1070Gly
XM_011535988.1:c.2071A>G	XP_011534290.1:p.Arg691Gly
NM_001346813.1:c.4930A>G	NP_001333742.1:p.Arg1644Gly
NM_001363725.1:c.2680A>G	NP_001350654.1:p.Arg894Gly
XM_011535984.2:c.5140A>G	XP_011534286.2:p.Arg1714Gly
XM_011535988.3:c.2071A>G	XP_011534290.1:p.Arg691Gly
XM_017011103.2:c.5041A>G	XP_016866592.1:p.Arg1681Gly
XM_017011104.1:c.5011A>G	XP_016866593.1:p.Arg1671Gly
XM_017011105.2:c.4981A>G	XP_016866594.1:p.Arg1661Gly
XM_017011106.2:c.4852A>G	XP_016866595.1:p.Arg1618Gly
XM_017011107.2:c.4831A>G	XP_016866596.1:p.Arg1611Gly
XR_002956289.1:n.5126A>G
NM_001363725.2:c.2680A>G	NP_001350654.1:p.Arg894Gly
NM_001371656.1:c.5059A>G	NP_001358585.1:p.Arg1687Gly
NM_001374820.1:c.5059A>G	NP_001361749.1:p.Arg1687Gly
NM_001374828.1:c.5179A>G MANE Select	NP_001361757.1:p.Arg1727Gly
NM_017519.3:c.5020A>G	NP_059989.3:p.Arg1674Gly