Canonical Allele Identifier: CA366381170

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2016017
• ClinVar RCV Id: RCV002843689
• gnomAD v4: 6-156778048-C-G
• MyVariant Identifiers: chr6:g.157099182C>G (hg19) ; chr6:g.156778048C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156778048C>G , CM000668.2:g.156778048C>G	GRCh38
NC_000006.11:g.157099182C>G , CM000668.1:g.157099182C>G	GRCh37
NC_000006.10:g.157140874C>G	NCBI36
NG_032093.1:g.5119C>G
NG_032093.2:g.5119C>G
NG_066624.1:g.7023C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.368C>G	ENSP00000055163.8:p.Ser123Cys
ENST00000414678.8:c.368C>G	ENSP00000412835.3:p.Ser123Cys
ENST00000637015.2:c.368C>G	ENSP00000489729.2:p.Ser123Cys
ENST00000346085.10:c.368C>G	ENSP00000344546.5:p.Ser123Cys
ENST00000350026.10:c.119C>G	ENSP00000055163.7:p.Ser40Cys
ENST00000636930.2:c.368C>G MANE Select	ENSP00000490491.2:p.Ser123Cys
ENST00000647938.1:c.119C>G	ENSP00000498155.1:p.Ser40Cys
ENST00000674298.1:c.108C>G
ENST00000346085.9:c.119C>G	ENSP00000344546.4:p.Ser40Cys
ENST00000350026.9:c.119C>G	ENSP00000055163.7:p.Ser40Cys
NM_017519.2:c.119C>G	NP_059989.2:p.Ser40Cys
NM_020732.3:c.119C>G	NP_065783.3:p.Ser40Cys
XM_005267069.3:c.119C>G	XP_005267126.2:p.Ser40Cys
XR_943148.1:n.177+198G>C
NM_001346813.1:c.119C>G	NP_001333742.1:p.Ser40Cys
XM_011535984.2:c.119C>G	XP_011534286.2:p.Ser40Cys
XM_017011103.2:c.119C>G	XP_016866592.1:p.Ser40Cys
XM_017011104.1:c.119C>G	XP_016866593.1:p.Ser40Cys
XM_017011105.2:c.119C>G	XP_016866594.1:p.Ser40Cys
XM_017011106.2:c.119C>G	XP_016866595.1:p.Ser40Cys
XM_017011107.2:c.119C>G	XP_016866596.1:p.Ser40Cys
XR_002956289.1:n.202C>G
NM_001371656.1:c.368C>G	NP_001358585.1:p.Ser123Cys
NM_001374820.1:c.368C>G	NP_001361749.1:p.Ser123Cys
NM_001374828.1:c.368C>G MANE Select	NP_001361757.1:p.Ser123Cys
NM_017519.3:c.368C>G	NP_059989.3:p.Ser123Cys
NR_163974.1:n.273+198G>C