Canonical Allele Identifier: CA2499218172

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1184937
• ClinVar RCV Id: RCV002464466
• dbSNP Id: rs2128374526

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201095dup , CM000668.2:g.157201095dup	GRCh38
NC_000006.11:g.157522229dup , CM000668.1:g.157522229dup	GRCh37
NC_000006.10:g.157563921dup	NCBI36
NG_032093.1:g.428166dup
NG_032093.2:g.428166dup
NG_066624.1:g.430070dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4711dup	ENSP00000055163.8:p.Val1571GlyfsTer9
ENST00000414678.8:c.4780dup	ENSP00000412835.3:p.Val1594GlyfsTer9
ENST00000637015.2:c.4999dup	ENSP00000489729.2:p.Val1667GlyfsTer9
ENST00000346085.10:c.4750dup	ENSP00000344546.5:p.Val1584GlyfsTer9
ENST00000350026.10:c.4462dup	ENSP00000055163.7:p.Val1488GlyfsTer9
ENST00000414678.7:c.3028dup	ENSP00000412835.2:p.Val1010GlyfsTer9
ENST00000635849.1:c.2191dup	ENSP00000490948.1:p.Val731GlyfsTer9
ENST00000635957.1:c.1822dup	ENSP00000490385.1:p.Val608GlyfsTer9
ENST00000636227.1:n.3333dup
ENST00000636254.1:n.790dup
ENST00000636930.2:c.4870dup MANE Select	ENSP00000490491.2:p.Val1624GlyfsTer9
ENST00000636940.1:n.2867dup
ENST00000637015.1:c.2238dup
ENST00000637568.1:c.2152dup
ENST00000637741.1:n.1536dup
ENST00000637810.1:c.2212dup	ENSP00000489636.1:p.Val738GlyfsTer9
ENST00000637904.1:c.2371dup	ENSP00000490550.1:p.Val791GlyfsTer9
ENST00000647938.1:c.4501dup	ENSP00000498155.1:p.Val1501GlyfsTer9
ENST00000346085.9:c.4501dup	ENSP00000344546.4:p.Val1501GlyfsTer9
ENST00000350026.9:c.4462dup	ENSP00000055163.7:p.Val1488GlyfsTer9
ENST00000414678.6:c.3028dup	ENSP00000412835.2:p.Val1010GlyfsTer9
NM_017519.2:c.4462dup	NP_059989.2:p.Val1488GlyfsTer9
NM_020732.3:c.4501dup	NP_065783.3:p.Val1501GlyfsTer9
XM_005267069.3:c.4621dup	XP_005267126.2:p.Val1541GlyfsTer9
XM_011535984.1:c.3700dup	XP_011534286.1:p.Val1234GlyfsTer9
XM_011535985.1:c.3520dup	XP_011534287.1:p.Val1174GlyfsTer9
XM_011535986.1:c.3280dup	XP_011534288.1:p.Val1094GlyfsTer9
XM_011535987.1:c.2899dup	XP_011534289.1:p.Val967GlyfsTer9
XM_011535988.1:c.1762dup	XP_011534290.1:p.Val588GlyfsTer9
NM_001346813.1:c.4621dup	NP_001333742.1:p.Val1541GlyfsTer9
NM_001363725.1:c.2371dup	NP_001350654.1:p.Val791GlyfsTer9
XM_011535984.2:c.4831dup	XP_011534286.2:p.Val1611GlyfsTer9
XM_011535988.3:c.1762dup	XP_011534290.1:p.Val588GlyfsTer9
XM_017011103.2:c.4732dup	XP_016866592.1:p.Val1578GlyfsTer9
XM_017011104.1:c.4702dup	XP_016866593.1:p.Val1568GlyfsTer9
XM_017011105.2:c.4672dup	XP_016866594.1:p.Val1558GlyfsTer9
XM_017011106.2:c.4543dup	XP_016866595.1:p.Val1515GlyfsTer9
XM_017011107.2:c.4522dup	XP_016866596.1:p.Val1508GlyfsTer9
XR_002956289.1:n.4817dup
NM_001363725.2:c.2371dup	NP_001350654.1:p.Val791GlyfsTer9
NM_001371656.1:c.4750dup	NP_001358585.1:p.Val1584GlyfsTer9
NM_001374820.1:c.4750dup	NP_001361749.1:p.Val1584GlyfsTer9
NM_001374828.1:c.4870dup MANE Select	NP_001361757.1:p.Val1624GlyfsTer9
NM_017519.3:c.4711dup	NP_059989.3:p.Val1571GlyfsTer9