Canonical Allele Identifier: CA571903941

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 694703
• ClinVar RCV Id: RCV000856776 ; RCV001664485 ; RCV002453934 ; RCV001533122
• dbSNP Id: rs1289067120
• gnomAD v2: 6-157510805-A-AC
• MyVariant Identifiers: chr6:g.157510805_157510806insC (hg19) ; chr6:g.157189671_157189672insC (hg38)
• PubMed: PMID:23160955 ; PMID:25363768

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189677dup , CM000668.2:g.157189677dup	GRCh38
NC_000006.11:g.157510811dup , CM000668.1:g.157510811dup	GRCh37
NC_000006.10:g.157552503dup	NCBI36
NG_032093.1:g.416748dup
NG_032093.2:g.416748dup
NG_066624.1:g.418652dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3796dup	ENSP00000055163.8:p.Gln1266ProfsTer14
ENST00000414678.8:c.3865dup	ENSP00000412835.3:p.Gln1289ProfsTer14
ENST00000637015.2:c.4084dup	ENSP00000489729.2:p.Gln1362ProfsTer14
ENST00000346085.10:c.3835dup	ENSP00000344546.5:p.Gln1279ProfsTer14
ENST00000350026.10:c.3547dup	ENSP00000055163.7:p.Gln1183ProfsTer14
ENST00000414678.7:c.2113dup	ENSP00000412835.2:p.Gln705ProfsTer14
ENST00000635849.1:c.1276dup	ENSP00000490948.1:p.Gln426ProfsTer14
ENST00000635957.1:c.910dup	ENSP00000490385.1:p.Gln304ProfsTer14
ENST00000636930.2:c.3955dup MANE Select	ENSP00000490491.2:p.Gln1319ProfsTer14
ENST00000636940.1:n.1952dup
ENST00000637015.1:c.1323dup
ENST00000637568.1:c.1237dup
ENST00000637741.1:n.621dup
ENST00000637810.1:c.1297dup	ENSP00000489636.1:p.Gln433ProfsTer14
ENST00000637904.1:c.1456dup	ENSP00000490550.1:p.Gln486ProfsTer14
ENST00000647938.1:c.3586dup	ENSP00000498155.1:p.Gln1196ProfsTer14
ENST00000346085.9:c.3586dup	ENSP00000344546.4:p.Gln1196ProfsTer14
ENST00000350026.9:c.3547dup	ENSP00000055163.7:p.Gln1183ProfsTer14
ENST00000414678.6:c.2113dup	ENSP00000412835.2:p.Gln705ProfsTer14
NM_017519.2:c.3547dup	NP_059989.2:p.Gln1183ProfsTer14
NM_020732.3:c.3586dup	NP_065783.3:p.Gln1196ProfsTer14
XM_005267069.3:c.3706dup	XP_005267126.2:p.Gln1236ProfsTer14
XM_011535984.1:c.2785dup	XP_011534286.1:p.Gln929ProfsTer14
XM_011535985.1:c.2605dup	XP_011534287.1:p.Gln869ProfsTer14
XM_011535986.1:c.2365dup	XP_011534288.1:p.Gln789ProfsTer14
XM_011535987.1:c.1984dup	XP_011534289.1:p.Gln662ProfsTer14
XM_011535988.1:c.847dup	XP_011534290.1:p.Gln283ProfsTer14
NM_001346813.1:c.3706dup	NP_001333742.1:p.Gln1236ProfsTer14
NM_001363725.1:c.1456dup	NP_001350654.1:p.Gln486ProfsTer14
XM_011535984.2:c.3916dup	XP_011534286.2:p.Gln1306ProfsTer14
XM_011535988.3:c.847dup	XP_011534290.1:p.Gln283ProfsTer14
XM_017011103.2:c.3817dup	XP_016866592.1:p.Gln1273ProfsTer14
XM_017011104.1:c.3787dup	XP_016866593.1:p.Gln1263ProfsTer14
XM_017011105.2:c.3757dup	XP_016866594.1:p.Gln1253ProfsTer14
XM_017011106.2:c.3628dup	XP_016866595.1:p.Gln1210ProfsTer14
XM_017011107.2:c.3607dup	XP_016866596.1:p.Gln1203ProfsTer14
XR_002956289.1:n.3999dup
NM_001363725.2:c.1456dup	NP_001350654.1:p.Gln486ProfsTer14
NM_001371656.1:c.3835dup	NP_001358585.1:p.Gln1279ProfsTer14
NM_001374820.1:c.3835dup	NP_001361749.1:p.Gln1279ProfsTer14
NM_001374828.1:c.3955dup MANE Select	NP_001361757.1:p.Gln1319ProfsTer14
NM_017519.3:c.3796dup	NP_059989.3:p.Gln1266ProfsTer14