Canonical Allele Identifier: CA366242808

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 521742
• ClinVar RCV Id: RCV000622548 ; RCV001860450
• dbSNP Id: rs1329932861
• gnomAD v2: 6-157522508-G-A
• gnomAD v3: 6-157201374-G-A
• gnomAD v4: 6-157201374-G-A
• MyVariant Identifiers: chr6:g.157522508G>A (hg19) ; chr6:g.157201374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201374G>A , CM000668.2:g.157201374G>A	GRCh38
NC_000006.11:g.157522508G>A , CM000668.1:g.157522508G>A	GRCh37
NC_000006.10:g.157564200G>A	NCBI36
NG_032093.1:g.428445G>A
NG_032093.2:g.428445G>A
NG_066624.1:g.430349G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4990G>A	ENSP00000055163.8:p.Gly1664Arg
ENST00000414678.8:c.5059G>A	ENSP00000412835.3:p.Gly1687Arg
ENST00000637015.2:c.5278G>A	ENSP00000489729.2:p.Gly1760Arg
ENST00000346085.10:c.5029G>A	ENSP00000344546.5:p.Gly1677Arg
ENST00000350026.10:c.4741G>A	ENSP00000055163.7:p.Gly1581Arg
ENST00000414678.7:c.3307G>A	ENSP00000412835.2:p.Gly1103Arg
ENST00000635849.1:c.2470G>A	ENSP00000490948.1:p.Gly824Arg
ENST00000635957.1:c.2101G>A	ENSP00000490385.1:p.Gly701Arg
ENST00000636227.1:n.3612G>A
ENST00000636254.1:n.1069G>A
ENST00000636930.2:c.5149G>A MANE Select	ENSP00000490491.2:p.Gly1717Arg
ENST00000636940.1:n.3146G>A
ENST00000637015.1:c.2517G>A
ENST00000637568.1:c.2431G>A
ENST00000637741.1:n.1815G>A
ENST00000637810.1:c.2491G>A	ENSP00000489636.1:p.Gly831Arg
ENST00000637904.1:c.2650G>A	ENSP00000490550.1:p.Gly884Arg
ENST00000647938.1:c.4780G>A	ENSP00000498155.1:p.Gly1594Arg
ENST00000346085.9:c.4780G>A	ENSP00000344546.4:p.Gly1594Arg
ENST00000350026.9:c.4741G>A	ENSP00000055163.7:p.Gly1581Arg
ENST00000414678.6:c.3307G>A	ENSP00000412835.2:p.Gly1103Arg
NM_017519.2:c.4741G>A	NP_059989.2:p.Gly1581Arg
NM_020732.3:c.4780G>A	NP_065783.3:p.Gly1594Arg
XM_005267069.3:c.4900G>A	XP_005267126.2:p.Gly1634Arg
XM_011535984.1:c.3979G>A	XP_011534286.1:p.Gly1327Arg
XM_011535985.1:c.3799G>A	XP_011534287.1:p.Gly1267Arg
XM_011535986.1:c.3559G>A	XP_011534288.1:p.Gly1187Arg
XM_011535987.1:c.3178G>A	XP_011534289.1:p.Gly1060Arg
XM_011535988.1:c.2041G>A	XP_011534290.1:p.Gly681Arg
NM_001346813.1:c.4900G>A	NP_001333742.1:p.Gly1634Arg
NM_001363725.1:c.2650G>A	NP_001350654.1:p.Gly884Arg
XM_011535984.2:c.5110G>A	XP_011534286.2:p.Gly1704Arg
XM_011535988.3:c.2041G>A	XP_011534290.1:p.Gly681Arg
XM_017011103.2:c.5011G>A	XP_016866592.1:p.Gly1671Arg
XM_017011104.1:c.4981G>A	XP_016866593.1:p.Gly1661Arg
XM_017011105.2:c.4951G>A	XP_016866594.1:p.Gly1651Arg
XM_017011106.2:c.4822G>A	XP_016866595.1:p.Gly1608Arg
XM_017011107.2:c.4801G>A	XP_016866596.1:p.Gly1601Arg
XR_002956289.1:n.5096G>A
NM_001363725.2:c.2650G>A	NP_001350654.1:p.Gly884Arg
NM_001371656.1:c.5029G>A	NP_001358585.1:p.Gly1677Arg
NM_001374820.1:c.5029G>A	NP_001361749.1:p.Gly1677Arg
NM_001374828.1:c.5149G>A MANE Select	NP_001361757.1:p.Gly1717Arg
NM_017519.3:c.4990G>A	NP_059989.3:p.Gly1664Arg