Canonical Allele Identifier: CA4067514

Gene: ARID1B

Linked Data

• dbSNP Id: rs574296429
• ExAC: 6:157511174 G / A
• gnomAD v2: 6-157511174-G-A
• gnomAD v3: 6-157190040-G-A
• gnomAD v4: 6-157190040-G-A
• MyVariant Identifiers: chr6:g.157511174G>A (hg19) ; chr6:g.157190040G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190040G>A , CM000668.2:g.157190040G>A	GRCh38
NC_000006.11:g.157511174G>A , CM000668.1:g.157511174G>A	GRCh37
NC_000006.10:g.157552866G>A	NCBI36
NG_032093.1:g.417111G>A
NG_032093.2:g.417111G>A
NG_066624.1:g.419015G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3902G>A	ENSP00000055163.8:p.Ser1301Asn
ENST00000414678.8:c.3971G>A	ENSP00000412835.3:p.Ser1324Asn
ENST00000637015.2:c.4190G>A	ENSP00000489729.2:p.Ser1397Asn
ENST00000346085.10:c.3941G>A	ENSP00000344546.5:p.Ser1314Asn
ENST00000350026.10:c.3653G>A	ENSP00000055163.7:p.Ser1218Asn
ENST00000414678.7:c.2219G>A	ENSP00000412835.2:p.Ser740Asn
ENST00000635849.1:c.1382G>A	ENSP00000490948.1:p.Ser461Asn
ENST00000635957.1:c.1014-1G>A	ENSP00000490385.1:n.1014-1G>A
ENST00000636930.2:c.4061G>A MANE Select	ENSP00000490491.2:p.Ser1354Asn
ENST00000636940.1:n.2058G>A
ENST00000637015.1:c.1429G>A
ENST00000637568.1:c.1343G>A
ENST00000637741.1:n.727G>A
ENST00000637810.1:c.1403G>A	ENSP00000489636.1:p.Ser468Asn
ENST00000637904.1:c.1562G>A	ENSP00000490550.1:p.Ser521Asn
ENST00000647938.1:c.3692G>A	ENSP00000498155.1:p.Ser1231Asn
ENST00000346085.9:c.3692G>A	ENSP00000344546.4:p.Ser1231Asn
ENST00000350026.9:c.3653G>A	ENSP00000055163.7:p.Ser1218Asn
ENST00000414678.6:c.2219G>A	ENSP00000412835.2:p.Ser740Asn
NM_017519.2:c.3653G>A	NP_059989.2:p.Ser1218Asn
NM_020732.3:c.3692G>A	NP_065783.3:p.Ser1231Asn
XM_005267069.3:c.3812G>A	XP_005267126.2:p.Ser1271Asn
XM_011535984.1:c.2891G>A	XP_011534286.1:p.Ser964Asn
XM_011535985.1:c.2711G>A	XP_011534287.1:p.Ser904Asn
XM_011535986.1:c.2471G>A	XP_011534288.1:p.Ser824Asn
XM_011535987.1:c.2090G>A	XP_011534289.1:p.Ser697Asn
XM_011535988.1:c.953G>A	XP_011534290.1:p.Ser318Asn
NM_001346813.1:c.3812G>A	NP_001333742.1:p.Ser1271Asn
NM_001363725.1:c.1562G>A	NP_001350654.1:p.Ser521Asn
XM_011535984.2:c.4022G>A	XP_011534286.2:p.Ser1341Asn
XM_011535988.3:c.953G>A	XP_011534290.1:p.Ser318Asn
XM_017011103.2:c.3923G>A	XP_016866592.1:p.Ser1308Asn
XM_017011104.1:c.3893G>A	XP_016866593.1:p.Ser1298Asn
XM_017011105.2:c.3863G>A	XP_016866594.1:p.Ser1288Asn
XM_017011106.2:c.3734G>A	XP_016866595.1:p.Ser1245Asn
XM_017011107.2:c.3713G>A	XP_016866596.1:p.Ser1238Asn
XR_002956289.1:n.4105G>A
NM_001363725.2:c.1562G>A	NP_001350654.1:p.Ser521Asn
NM_001371656.1:c.3941G>A	NP_001358585.1:p.Ser1314Asn
NM_001374820.1:c.3941G>A	NP_001361749.1:p.Ser1314Asn
NM_001374828.1:c.4061G>A MANE Select	NP_001361757.1:p.Ser1354Asn
NM_017519.3:c.3902G>A	NP_059989.3:p.Ser1301Asn