Canonical Allele Identifier: CA16042661

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 372882
• ClinVar RCV Id: RCV000413516 ; RCV001336508 ; RCV001533090
• dbSNP Id: rs1057518045
• COSMIC: COSM5928775 ; COSM5928776
• MyVariant Identifiers: chr6:g.157431695G>A (hg19) ; chr6:g.157110561G>A (hg38)
• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157110561G>A , CM000668.2:g.157110561G>A	GRCh38
NC_000006.11:g.157431695G>A , CM000668.1:g.157431695G>A	GRCh37
NC_000006.10:g.157473387G>A	NCBI36
NG_032093.1:g.337632G>A
NG_032093.2:g.337632G>A
NG_066624.1:g.339536G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2581G>A	ENSP00000055163.8:p.Gly861Ser
ENST00000414678.8:c.2492-22467G>A	ENSP00000412835.3:n.2492-22467G>A
ENST00000637015.2:c.2581G>A	ENSP00000489729.2:p.Gly861Ser
ENST00000319584.11:c.595G>A	ENSP00000313006.7:p.Gly199Ser
ENST00000346085.10:c.2620G>A	ENSP00000344546.5:p.Gly874Ser
ENST00000350026.10:c.2332G>A	ENSP00000055163.7:p.Gly778Ser
ENST00000414678.7:c.740-22467G>A	ENSP00000412835.2:n.740-22467G>A
ENST00000452544.2:n.482G>A
ENST00000493658.2:n.230G>A
ENST00000635849.1:c.82G>A	ENSP00000490948.1:p.Gly28Ser
ENST00000636930.2:c.2581G>A MANE Select	ENSP00000490491.2:p.Gly861Ser
ENST00000637003.1:c.82G>A	ENSP00000489666.1:p.Gly28Ser
ENST00000637810.1:c.82G>A	ENSP00000489636.1:p.Gly28Ser
ENST00000637904.1:c.82G>A	ENSP00000490550.1:p.Gly28Ser
ENST00000647938.1:c.2371G>A	ENSP00000498155.1:p.Gly791Ser
ENST00000674190.1:n.1330G>A
ENST00000319584.10:c.598G>A	ENSP00000313006.6:p.Gly200Ser
ENST00000346085.9:c.2371G>A	ENSP00000344546.4:p.Gly791Ser
ENST00000350026.9:c.2332G>A	ENSP00000055163.7:p.Gly778Ser
ENST00000414678.6:c.740-22467G>A	ENSP00000412835.2:n.740-22467G>A
ENST00000452544.1:n.440G>A
ENST00000493658.1:n.230G>A
NM_017519.2:c.2332G>A	NP_059989.2:p.Gly778Ser
NM_020732.3:c.2371G>A	NP_065783.3:p.Gly791Ser
XM_005267069.3:c.2332G>A	XP_005267126.2:p.Gly778Ser
XM_011535984.1:c.1282G>A	XP_011534286.1:p.Gly428Ser
XM_011535985.1:c.1282G>A	XP_011534287.1:p.Gly428Ser
XM_011535986.1:c.862G>A	XP_011534288.1:p.Gly288Ser
XM_011535987.1:c.481G>A	XP_011534289.1:p.Gly161Ser
NM_001346813.1:c.2332G>A	NP_001333742.1:p.Gly778Ser
NM_001363725.1:c.82G>A	NP_001350654.1:p.Gly28Ser
XM_011535984.2:c.2413G>A	XP_011534286.2:p.Gly805Ser
XM_017011103.2:c.2413G>A	XP_016866592.1:p.Gly805Ser
XM_017011104.1:c.2413G>A	XP_016866593.1:p.Gly805Ser
XM_017011105.2:c.2413G>A	XP_016866594.1:p.Gly805Ser
XM_017011106.2:c.2413G>A	XP_016866595.1:p.Gly805Ser
XM_017011107.2:c.2413G>A	XP_016866596.1:p.Gly805Ser
XR_002956289.1:n.2496G>A
NM_001363725.2:c.82G>A	NP_001350654.1:p.Gly28Ser
NM_001371656.1:c.2620G>A	NP_001358585.1:p.Gly874Ser
NM_001374820.1:c.2620G>A	NP_001361749.1:p.Gly874Ser
NM_001374828.1:c.2581G>A MANE Select	NP_001361757.1:p.Gly861Ser
NM_017519.3:c.2581G>A	NP_059989.3:p.Gly861Ser