Canonical Allele Identifier: CA366242739

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 3129402
• ClinVar RCV Id: RCV004425268
• MyVariant Identifiers: chr6:g.157522494C>T (hg19) ; chr6:g.157201360C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201360C>T , CM000668.2:g.157201360C>T	GRCh38
NC_000006.11:g.157522494C>T , CM000668.1:g.157522494C>T	GRCh37
NC_000006.10:g.157564186C>T	NCBI36
NG_032093.1:g.428431C>T
NG_032093.2:g.428431C>T
NG_066624.1:g.430335C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4976C>T	ENSP00000055163.8:p.Thr1659Ile
ENST00000414678.8:c.5045C>T	ENSP00000412835.3:p.Thr1682Ile
ENST00000637015.2:c.5264C>T	ENSP00000489729.2:p.Thr1755Ile
ENST00000346085.10:c.5015C>T	ENSP00000344546.5:p.Thr1672Ile
ENST00000350026.10:c.4727C>T	ENSP00000055163.7:p.Thr1576Ile
ENST00000414678.7:c.3293C>T	ENSP00000412835.2:p.Thr1098Ile
ENST00000635849.1:c.2456C>T	ENSP00000490948.1:p.Thr819Ile
ENST00000635957.1:c.2087C>T	ENSP00000490385.1:p.Thr696Ile
ENST00000636227.1:n.3598C>T
ENST00000636254.1:n.1055C>T
ENST00000636930.2:c.5135C>T MANE Select	ENSP00000490491.2:p.Thr1712Ile
ENST00000636940.1:n.3132C>T
ENST00000637015.1:c.2503C>T
ENST00000637568.1:c.2417C>T
ENST00000637741.1:n.1801C>T
ENST00000637810.1:c.2477C>T	ENSP00000489636.1:p.Thr826Ile
ENST00000637904.1:c.2636C>T	ENSP00000490550.1:p.Thr879Ile
ENST00000647938.1:c.4766C>T	ENSP00000498155.1:p.Thr1589Ile
ENST00000346085.9:c.4766C>T	ENSP00000344546.4:p.Thr1589Ile
ENST00000350026.9:c.4727C>T	ENSP00000055163.7:p.Thr1576Ile
ENST00000414678.6:c.3293C>T	ENSP00000412835.2:p.Thr1098Ile
NM_017519.2:c.4727C>T	NP_059989.2:p.Thr1576Ile
NM_020732.3:c.4766C>T	NP_065783.3:p.Thr1589Ile
XM_005267069.3:c.4886C>T	XP_005267126.2:p.Thr1629Ile
XM_011535984.1:c.3965C>T	XP_011534286.1:p.Thr1322Ile
XM_011535985.1:c.3785C>T	XP_011534287.1:p.Thr1262Ile
XM_011535986.1:c.3545C>T	XP_011534288.1:p.Thr1182Ile
XM_011535987.1:c.3164C>T	XP_011534289.1:p.Thr1055Ile
XM_011535988.1:c.2027C>T	XP_011534290.1:p.Thr676Ile
NM_001346813.1:c.4886C>T	NP_001333742.1:p.Thr1629Ile
NM_001363725.1:c.2636C>T	NP_001350654.1:p.Thr879Ile
XM_011535984.2:c.5096C>T	XP_011534286.2:p.Thr1699Ile
XM_011535988.3:c.2027C>T	XP_011534290.1:p.Thr676Ile
XM_017011103.2:c.4997C>T	XP_016866592.1:p.Thr1666Ile
XM_017011104.1:c.4967C>T	XP_016866593.1:p.Thr1656Ile
XM_017011105.2:c.4937C>T	XP_016866594.1:p.Thr1646Ile
XM_017011106.2:c.4808C>T	XP_016866595.1:p.Thr1603Ile
XM_017011107.2:c.4787C>T	XP_016866596.1:p.Thr1596Ile
XR_002956289.1:n.5082C>T
NM_001363725.2:c.2636C>T	NP_001350654.1:p.Thr879Ile
NM_001371656.1:c.5015C>T	NP_001358585.1:p.Thr1672Ile
NM_001374820.1:c.5015C>T	NP_001361749.1:p.Thr1672Ile
NM_001374828.1:c.5135C>T MANE Select	NP_001361757.1:p.Thr1712Ile
NM_017519.3:c.4976C>T	NP_059989.3:p.Thr1659Ile