Canonical Allele Identifier: CA366234208

Gene: ARID1B

Linked Data

• dbSNP Id: rs1473976074
• gnomAD v2: 6-157510878-C-T
• gnomAD v3: 6-157189744-C-T
• gnomAD v4: 6-157189744-C-T
• MyVariant Identifiers: chr6:g.157510878C>T (hg19) ; chr6:g.157189744C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189744C>T , CM000668.2:g.157189744C>T	GRCh38
NC_000006.11:g.157510878C>T , CM000668.1:g.157510878C>T	GRCh37
NC_000006.10:g.157552570C>T	NCBI36
NG_032093.1:g.416815C>T
NG_032093.2:g.416815C>T
NG_066624.1:g.418719C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3863C>T	ENSP00000055163.8:p.Thr1288Ile
ENST00000414678.8:c.3932C>T	ENSP00000412835.3:p.Thr1311Ile
ENST00000637015.2:c.4151C>T	ENSP00000489729.2:p.Thr1384Ile
ENST00000346085.10:c.3902C>T	ENSP00000344546.5:p.Thr1301Ile
ENST00000350026.10:c.3614C>T	ENSP00000055163.7:p.Thr1205Ile
ENST00000414678.7:c.2180C>T	ENSP00000412835.2:p.Thr727Ile
ENST00000635849.1:c.1343C>T	ENSP00000490948.1:p.Thr448Ile
ENST00000635957.1:c.977C>T	ENSP00000490385.1:p.Thr326Ile
ENST00000636930.2:c.4022C>T MANE Select	ENSP00000490491.2:p.Thr1341Ile
ENST00000636940.1:n.2019C>T
ENST00000637015.1:c.1390C>T
ENST00000637568.1:c.1304C>T
ENST00000637741.1:n.688C>T
ENST00000637810.1:c.1364C>T	ENSP00000489636.1:p.Thr455Ile
ENST00000637904.1:c.1523C>T	ENSP00000490550.1:p.Thr508Ile
ENST00000647938.1:c.3653C>T	ENSP00000498155.1:p.Thr1218Ile
ENST00000346085.9:c.3653C>T	ENSP00000344546.4:p.Thr1218Ile
ENST00000350026.9:c.3614C>T	ENSP00000055163.7:p.Thr1205Ile
ENST00000414678.6:c.2180C>T	ENSP00000412835.2:p.Thr727Ile
NM_017519.2:c.3614C>T	NP_059989.2:p.Thr1205Ile
NM_020732.3:c.3653C>T	NP_065783.3:p.Thr1218Ile
XM_005267069.3:c.3773C>T	XP_005267126.2:p.Thr1258Ile
XM_011535984.1:c.2852C>T	XP_011534286.1:p.Thr951Ile
XM_011535985.1:c.2672C>T	XP_011534287.1:p.Thr891Ile
XM_011535986.1:c.2432C>T	XP_011534288.1:p.Thr811Ile
XM_011535987.1:c.2051C>T	XP_011534289.1:p.Thr684Ile
XM_011535988.1:c.914C>T	XP_011534290.1:p.Thr305Ile
NM_001346813.1:c.3773C>T	NP_001333742.1:p.Thr1258Ile
NM_001363725.1:c.1523C>T	NP_001350654.1:p.Thr508Ile
XM_011535984.2:c.3983C>T	XP_011534286.2:p.Thr1328Ile
XM_011535988.3:c.914C>T	XP_011534290.1:p.Thr305Ile
XM_017011103.2:c.3884C>T	XP_016866592.1:p.Thr1295Ile
XM_017011104.1:c.3854C>T	XP_016866593.1:p.Thr1285Ile
XM_017011105.2:c.3824C>T	XP_016866594.1:p.Thr1275Ile
XM_017011106.2:c.3695C>T	XP_016866595.1:p.Thr1232Ile
XM_017011107.2:c.3674C>T	XP_016866596.1:p.Thr1225Ile
XR_002956289.1:n.4066C>T
NM_001363725.2:c.1523C>T	NP_001350654.1:p.Thr508Ile
NM_001371656.1:c.3902C>T	NP_001358585.1:p.Thr1301Ile
NM_001374820.1:c.3902C>T	NP_001361749.1:p.Thr1301Ile
NM_001374828.1:c.4022C>T MANE Select	NP_001361757.1:p.Thr1341Ile
NM_017519.3:c.3863C>T	NP_059989.3:p.Thr1288Ile