Canonical Allele Identifier: CA366239840

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366567
• gnomAD v4: 6-157198888-G-A
• MyVariant Identifiers: chr6:g.157520022G>A (hg19) ; chr6:g.157198888G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198888G>A , CM000668.2:g.157198888G>A	GRCh38
NC_000006.11:g.157520022G>A , CM000668.1:g.157520022G>A	GRCh37
NC_000006.10:g.157561714G>A	NCBI36
NG_032093.1:g.425959G>A
NG_032093.2:g.425959G>A
NG_066624.1:g.427863G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4301G>A	ENSP00000055163.8:p.Gly1434Asp
ENST00000414678.8:c.4370G>A	ENSP00000412835.3:p.Gly1457Asp
ENST00000637015.2:c.4589G>A	ENSP00000489729.2:p.Gly1530Asp
ENST00000346085.10:c.4340G>A	ENSP00000344546.5:p.Gly1447Asp
ENST00000350026.10:c.4052G>A	ENSP00000055163.7:p.Gly1351Asp
ENST00000414678.7:c.2618G>A	ENSP00000412835.2:p.Gly873Asp
ENST00000635849.1:c.1781G>A	ENSP00000490948.1:p.Gly594Asp
ENST00000635957.1:c.1412G>A	ENSP00000490385.1:p.Gly471Asp
ENST00000636227.1:n.2923G>A
ENST00000636254.1:n.380G>A
ENST00000636930.2:c.4460G>A MANE Select	ENSP00000490491.2:p.Gly1487Asp
ENST00000636940.1:n.2457G>A
ENST00000637015.1:c.1828G>A
ENST00000637568.1:c.1742G>A
ENST00000637741.1:n.1126G>A
ENST00000637810.1:c.1802G>A	ENSP00000489636.1:p.Gly601Asp
ENST00000637904.1:c.1961G>A	ENSP00000490550.1:p.Gly654Asp
ENST00000647938.1:c.4091G>A	ENSP00000498155.1:p.Gly1364Asp
ENST00000346085.9:c.4091G>A	ENSP00000344546.4:p.Gly1364Asp
ENST00000350026.9:c.4052G>A	ENSP00000055163.7:p.Gly1351Asp
ENST00000414678.6:c.2618G>A	ENSP00000412835.2:p.Gly873Asp
NM_017519.2:c.4052G>A	NP_059989.2:p.Gly1351Asp
NM_020732.3:c.4091G>A	NP_065783.3:p.Gly1364Asp
XM_005267069.3:c.4211G>A	XP_005267126.2:p.Gly1404Asp
XM_011535984.1:c.3290G>A	XP_011534286.1:p.Gly1097Asp
XM_011535985.1:c.3110G>A	XP_011534287.1:p.Gly1037Asp
XM_011535986.1:c.2870G>A	XP_011534288.1:p.Gly957Asp
XM_011535987.1:c.2489G>A	XP_011534289.1:p.Gly830Asp
XM_011535988.1:c.1352G>A	XP_011534290.1:p.Gly451Asp
NM_001346813.1:c.4211G>A	NP_001333742.1:p.Gly1404Asp
NM_001363725.1:c.1961G>A	NP_001350654.1:p.Gly654Asp
XM_011535984.2:c.4421G>A	XP_011534286.2:p.Gly1474Asp
XM_011535988.3:c.1352G>A	XP_011534290.1:p.Gly451Asp
XM_017011103.2:c.4322G>A	XP_016866592.1:p.Gly1441Asp
XM_017011104.1:c.4292G>A	XP_016866593.1:p.Gly1431Asp
XM_017011105.2:c.4262G>A	XP_016866594.1:p.Gly1421Asp
XM_017011106.2:c.4133G>A	XP_016866595.1:p.Gly1378Asp
XM_017011107.2:c.4112G>A	XP_016866596.1:p.Gly1371Asp
XR_002956289.1:n.4427-1817G>A
NM_001363725.2:c.1961G>A	NP_001350654.1:p.Gly654Asp
NM_001371656.1:c.4340G>A	NP_001358585.1:p.Gly1447Asp
NM_001374820.1:c.4340G>A	NP_001361749.1:p.Gly1447Asp
NM_001374828.1:c.4460G>A MANE Select	NP_001361757.1:p.Gly1487Asp
NM_017519.3:c.4301G>A	NP_059989.3:p.Gly1434Asp