Canonical Allele Identifier: CA1139771216

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1804915
• ClinVar RCV Id: RCV002471333

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201136dup , CM000668.2:g.157201136dup	GRCh38
NC_000006.11:g.157522270dup , CM000668.1:g.157522270dup	GRCh37
NC_000006.10:g.157563962dup	NCBI36
NG_032093.1:g.428207dup
NG_032093.2:g.428207dup
NG_066624.1:g.430111dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4752dup	ENSP00000055163.8:p.His1585SerfsTer?
ENST00000414678.8:c.4821dup	ENSP00000412835.3:p.His1608SerfsTer?
ENST00000637015.2:c.5040dup	ENSP00000489729.2:p.His1681SerfsTer?
ENST00000346085.10:c.4791dup	ENSP00000344546.5:p.His1598SerfsTer?
ENST00000350026.10:c.4503dup	ENSP00000055163.7:p.His1502SerfsTer?
ENST00000414678.7:c.3069dup	ENSP00000412835.2:p.His1024SerfsTer?
ENST00000635849.1:c.2232dup	ENSP00000490948.1:p.His745SerfsTer?
ENST00000635957.1:c.1863dup	ENSP00000490385.1:p.His622SerfsTer?
ENST00000636227.1:n.3374dup
ENST00000636254.1:n.831dup
ENST00000636930.2:c.4911dup MANE Select	ENSP00000490491.2:p.His1638SerfsTer?
ENST00000636940.1:n.2908dup
ENST00000637015.1:c.2279dup
ENST00000637568.1:c.2193dup
ENST00000637741.1:n.1577dup
ENST00000637810.1:c.2253dup	ENSP00000489636.1:p.His752SerfsTer?
ENST00000637904.1:c.2412dup	ENSP00000490550.1:p.His805SerfsTer?
ENST00000647938.1:c.4542dup	ENSP00000498155.1:p.His1515SerfsTer?
ENST00000346085.9:c.4542dup	ENSP00000344546.4:p.His1515SerfsTer?
ENST00000350026.9:c.4503dup	ENSP00000055163.7:p.His1502SerfsTer?
ENST00000414678.6:c.3069dup	ENSP00000412835.2:p.His1024SerfsTer?
NM_017519.2:c.4503dup	NP_059989.2:p.His1502SerfsTer?
NM_020732.3:c.4542dup	NP_065783.3:p.His1515SerfsTer?
XM_005267069.3:c.4662dup	XP_005267126.2:p.His1555SerfsTer?
XM_011535984.1:c.3741dup	XP_011534286.1:p.His1248SerfsTer?
XM_011535985.1:c.3561dup	XP_011534287.1:p.His1188SerfsTer?
XM_011535986.1:c.3321dup	XP_011534288.1:p.His1108SerfsTer?
XM_011535987.1:c.2940dup	XP_011534289.1:p.His981SerfsTer?
XM_011535988.1:c.1803dup	XP_011534290.1:p.His602SerfsTer?
NM_001346813.1:c.4662dup	NP_001333742.1:p.His1555SerfsTer?
NM_001363725.1:c.2412dup	NP_001350654.1:p.His805SerfsTer?
XM_011535984.2:c.4872dup	XP_011534286.2:p.His1625SerfsTer?
XM_011535988.3:c.1803dup	XP_011534290.1:p.His602SerfsTer?
XM_017011103.2:c.4773dup	XP_016866592.1:p.His1592SerfsTer?
XM_017011104.1:c.4743dup	XP_016866593.1:p.His1582SerfsTer?
XM_017011105.2:c.4713dup	XP_016866594.1:p.His1572SerfsTer?
XM_017011106.2:c.4584dup	XP_016866595.1:p.His1529SerfsTer?
XM_017011107.2:c.4563dup	XP_016866596.1:p.His1522SerfsTer?
XR_002956289.1:n.4858dup
NM_001363725.2:c.2412dup	NP_001350654.1:p.His805SerfsTer?
NM_001371656.1:c.4791dup	NP_001358585.1:p.His1598SerfsTer?
NM_001374820.1:c.4791dup	NP_001361749.1:p.His1598SerfsTer?
NM_001374828.1:c.4911dup MANE Select	NP_001361757.1:p.His1638SerfsTer?
NM_017519.3:c.4752dup	NP_059989.3:p.His1585SerfsTer?