Canonical Allele Identifier: CA366242326

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375455
• gnomAD v4: 6-157201248-A-G
• MyVariant Identifiers: chr6:g.157522382A>G (hg19) ; chr6:g.157201248A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201248A>G , CM000668.2:g.157201248A>G	GRCh38
NC_000006.11:g.157522382A>G , CM000668.1:g.157522382A>G	GRCh37
NC_000006.10:g.157564074A>G	NCBI36
NG_032093.1:g.428319A>G
NG_032093.2:g.428319A>G
NG_066624.1:g.430223A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4864A>G	ENSP00000055163.8:p.Arg1622Gly
ENST00000414678.8:c.4933A>G	ENSP00000412835.3:p.Arg1645Gly
ENST00000637015.2:c.5152A>G	ENSP00000489729.2:p.Arg1718Gly
ENST00000346085.10:c.4903A>G	ENSP00000344546.5:p.Arg1635Gly
ENST00000350026.10:c.4615A>G	ENSP00000055163.7:p.Arg1539Gly
ENST00000414678.7:c.3181A>G	ENSP00000412835.2:p.Arg1061Gly
ENST00000635849.1:c.2344A>G	ENSP00000490948.1:p.Arg782Gly
ENST00000635957.1:c.1975A>G	ENSP00000490385.1:p.Arg659Gly
ENST00000636227.1:n.3486A>G
ENST00000636254.1:n.943A>G
ENST00000636930.2:c.5023A>G MANE Select	ENSP00000490491.2:p.Arg1675Gly
ENST00000636940.1:n.3020A>G
ENST00000637015.1:c.2391A>G
ENST00000637568.1:c.2305A>G
ENST00000637741.1:n.1689A>G
ENST00000637810.1:c.2365A>G	ENSP00000489636.1:p.Arg789Gly
ENST00000637904.1:c.2524A>G	ENSP00000490550.1:p.Arg842Gly
ENST00000647938.1:c.4654A>G	ENSP00000498155.1:p.Arg1552Gly
ENST00000346085.9:c.4654A>G	ENSP00000344546.4:p.Arg1552Gly
ENST00000350026.9:c.4615A>G	ENSP00000055163.7:p.Arg1539Gly
ENST00000414678.6:c.3181A>G	ENSP00000412835.2:p.Arg1061Gly
NM_017519.2:c.4615A>G	NP_059989.2:p.Arg1539Gly
NM_020732.3:c.4654A>G	NP_065783.3:p.Arg1552Gly
XM_005267069.3:c.4774A>G	XP_005267126.2:p.Arg1592Gly
XM_011535984.1:c.3853A>G	XP_011534286.1:p.Arg1285Gly
XM_011535985.1:c.3673A>G	XP_011534287.1:p.Arg1225Gly
XM_011535986.1:c.3433A>G	XP_011534288.1:p.Arg1145Gly
XM_011535987.1:c.3052A>G	XP_011534289.1:p.Arg1018Gly
XM_011535988.1:c.1915A>G	XP_011534290.1:p.Arg639Gly
NM_001346813.1:c.4774A>G	NP_001333742.1:p.Arg1592Gly
NM_001363725.1:c.2524A>G	NP_001350654.1:p.Arg842Gly
XM_011535984.2:c.4984A>G	XP_011534286.2:p.Arg1662Gly
XM_011535988.3:c.1915A>G	XP_011534290.1:p.Arg639Gly
XM_017011103.2:c.4885A>G	XP_016866592.1:p.Arg1629Gly
XM_017011104.1:c.4855A>G	XP_016866593.1:p.Arg1619Gly
XM_017011105.2:c.4825A>G	XP_016866594.1:p.Arg1609Gly
XM_017011106.2:c.4696A>G	XP_016866595.1:p.Arg1566Gly
XM_017011107.2:c.4675A>G	XP_016866596.1:p.Arg1559Gly
XR_002956289.1:n.4970A>G
NM_001363725.2:c.2524A>G	NP_001350654.1:p.Arg842Gly
NM_001371656.1:c.4903A>G	NP_001358585.1:p.Arg1635Gly
NM_001374820.1:c.4903A>G	NP_001361749.1:p.Arg1635Gly
NM_001374828.1:c.5023A>G MANE Select	NP_001361757.1:p.Arg1675Gly
NM_017519.3:c.4864A>G	NP_059989.3:p.Arg1622Gly