Canonical Allele Identifier: CA366234835

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2337670
• ClinVar RCV Id: RCV003443156 ; RCV002949946
• dbSNP Id: rs1476545892
• gnomAD v3: 6-157190060-G-A
• gnomAD v4: 6-157190060-G-A
• MyVariant Identifiers: chr6:g.157511194G>A (hg19) ; chr6:g.157190060G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190060G>A , CM000668.2:g.157190060G>A	GRCh38
NC_000006.11:g.157511194G>A , CM000668.1:g.157511194G>A	GRCh37
NC_000006.10:g.157552886G>A	NCBI36
NG_032093.1:g.417131G>A
NG_032093.2:g.417131G>A
NG_066624.1:g.419035G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3922G>A	ENSP00000055163.8:p.Asp1308Asn
ENST00000414678.8:c.3991G>A	ENSP00000412835.3:p.Asp1331Asn
ENST00000637015.2:c.4210G>A	ENSP00000489729.2:p.Asp1404Asn
ENST00000346085.10:c.3961G>A	ENSP00000344546.5:p.Asp1321Asn
ENST00000350026.10:c.3673G>A	ENSP00000055163.7:p.Asp1225Asn
ENST00000414678.7:c.2239G>A	ENSP00000412835.2:p.Asp747Asn
ENST00000635849.1:c.1402G>A	ENSP00000490948.1:p.Asp468Asn
ENST00000635957.1:c.1033G>A	ENSP00000490385.1:p.Asp345Asn
ENST00000636930.2:c.4081G>A MANE Select	ENSP00000490491.2:p.Asp1361Asn
ENST00000636940.1:n.2078G>A
ENST00000637015.1:c.1449G>A
ENST00000637568.1:c.1363G>A
ENST00000637741.1:n.747G>A
ENST00000637810.1:c.1423G>A	ENSP00000489636.1:p.Asp475Asn
ENST00000637904.1:c.1582G>A	ENSP00000490550.1:p.Asp528Asn
ENST00000647938.1:c.3712G>A	ENSP00000498155.1:p.Asp1238Asn
ENST00000346085.9:c.3712G>A	ENSP00000344546.4:p.Asp1238Asn
ENST00000350026.9:c.3673G>A	ENSP00000055163.7:p.Asp1225Asn
ENST00000414678.6:c.2239G>A	ENSP00000412835.2:p.Asp747Asn
NM_017519.2:c.3673G>A	NP_059989.2:p.Asp1225Asn
NM_020732.3:c.3712G>A	NP_065783.3:p.Asp1238Asn
XM_005267069.3:c.3832G>A	XP_005267126.2:p.Asp1278Asn
XM_011535984.1:c.2911G>A	XP_011534286.1:p.Asp971Asn
XM_011535985.1:c.2731G>A	XP_011534287.1:p.Asp911Asn
XM_011535986.1:c.2491G>A	XP_011534288.1:p.Asp831Asn
XM_011535987.1:c.2110G>A	XP_011534289.1:p.Asp704Asn
XM_011535988.1:c.973G>A	XP_011534290.1:p.Asp325Asn
NM_001346813.1:c.3832G>A	NP_001333742.1:p.Asp1278Asn
NM_001363725.1:c.1582G>A	NP_001350654.1:p.Asp528Asn
XM_011535984.2:c.4042G>A	XP_011534286.2:p.Asp1348Asn
XM_011535988.3:c.973G>A	XP_011534290.1:p.Asp325Asn
XM_017011103.2:c.3943G>A	XP_016866592.1:p.Asp1315Asn
XM_017011104.1:c.3913G>A	XP_016866593.1:p.Asp1305Asn
XM_017011105.2:c.3883G>A	XP_016866594.1:p.Asp1295Asn
XM_017011106.2:c.3754G>A	XP_016866595.1:p.Asp1252Asn
XM_017011107.2:c.3733G>A	XP_016866596.1:p.Asp1245Asn
XR_002956289.1:n.4125G>A
NM_001363725.2:c.1582G>A	NP_001350654.1:p.Asp528Asn
NM_001371656.1:c.3961G>A	NP_001358585.1:p.Asp1321Asn
NM_001374820.1:c.3961G>A	NP_001361749.1:p.Asp1321Asn
NM_001374828.1:c.4081G>A MANE Select	NP_001361757.1:p.Asp1361Asn
NM_017519.3:c.3922G>A	NP_059989.3:p.Asp1308Asn