Canonical Allele Identifier: CA366234583

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2876626
• ClinVar RCV Id: RCV003710397
• MyVariant Identifiers: chr6:g.157511174G>C (hg19) ; chr6:g.157190040G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3902G>C	ENSP00000055163.8:p.Ser1301Thr
ENST00000414678.8:c.3971G>C	ENSP00000412835.3:p.Ser1324Thr
ENST00000637015.2:c.4190G>C	ENSP00000489729.2:p.Ser1397Thr
ENST00000346085.10:c.3941G>C	ENSP00000344546.5:p.Ser1314Thr
ENST00000350026.10:c.3653G>C	ENSP00000055163.7:p.Ser1218Thr
ENST00000414678.7:c.2219G>C	ENSP00000412835.2:p.Ser740Thr
ENST00000635849.1:c.1382G>C	ENSP00000490948.1:p.Ser461Thr
ENST00000635957.1:c.1014-1G>C	ENSP00000490385.1:n.1014-1G>C
ENST00000636930.2:c.4061G>C MANE Select	ENSP00000490491.2:p.Ser1354Thr
ENST00000636940.1:n.2058G>C
ENST00000637015.1:c.1429G>C
ENST00000637568.1:c.1343G>C
ENST00000637741.1:n.727G>C
ENST00000637810.1:c.1403G>C	ENSP00000489636.1:p.Ser468Thr
ENST00000637904.1:c.1562G>C	ENSP00000490550.1:p.Ser521Thr
ENST00000647938.1:c.3692G>C	ENSP00000498155.1:p.Ser1231Thr
ENST00000346085.9:c.3692G>C	ENSP00000344546.4:p.Ser1231Thr
ENST00000350026.9:c.3653G>C	ENSP00000055163.7:p.Ser1218Thr
ENST00000414678.6:c.2219G>C	ENSP00000412835.2:p.Ser740Thr
NM_017519.2:c.3653G>C	NP_059989.2:p.Ser1218Thr
NM_020732.3:c.3692G>C	NP_065783.3:p.Ser1231Thr
XM_005267069.3:c.3812G>C	XP_005267126.2:p.Ser1271Thr
XM_011535984.1:c.2891G>C	XP_011534286.1:p.Ser964Thr
XM_011535985.1:c.2711G>C	XP_011534287.1:p.Ser904Thr
XM_011535986.1:c.2471G>C	XP_011534288.1:p.Ser824Thr
XM_011535987.1:c.2090G>C	XP_011534289.1:p.Ser697Thr
XM_011535988.1:c.953G>C	XP_011534290.1:p.Ser318Thr
NM_001346813.1:c.3812G>C	NP_001333742.1:p.Ser1271Thr
NM_001363725.1:c.1562G>C	NP_001350654.1:p.Ser521Thr
XM_011535984.2:c.4022G>C	XP_011534286.2:p.Ser1341Thr
XM_011535988.3:c.953G>C	XP_011534290.1:p.Ser318Thr
XM_017011103.2:c.3923G>C	XP_016866592.1:p.Ser1308Thr
XM_017011104.1:c.3893G>C	XP_016866593.1:p.Ser1298Thr
XM_017011105.2:c.3863G>C	XP_016866594.1:p.Ser1288Thr
XM_017011106.2:c.3734G>C	XP_016866595.1:p.Ser1245Thr
XM_017011107.2:c.3713G>C	XP_016866596.1:p.Ser1238Thr
XR_002956289.1:n.4105G>C
NM_001363725.2:c.1562G>C	NP_001350654.1:p.Ser521Thr
NM_001371656.1:c.3941G>C	NP_001358585.1:p.Ser1314Thr
NM_001374820.1:c.3941G>C	NP_001361749.1:p.Ser1314Thr
NM_001374828.1:c.4061G>C MANE Select	NP_001361757.1:p.Ser1354Thr
NM_017519.3:c.3902G>C	NP_059989.3:p.Ser1301Thr