Canonical Allele Identifier: CA707668

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 2202731
• ClinVar RCV Id: RCV002664155
• dbSNP Id: rs747674955
• ExAC: 1:27105698 G / T
• gnomAD v2: 1-27105698-G-T
• gnomAD v3: 1-26779207-G-T
• gnomAD v4: 1-26779207-G-T
• MyVariant Identifiers: chr1:g.27105698G>T (hg19) ; chr1:g.26779207G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779207G>T , CM000663.2:g.26779207G>T	GRCh38
NC_000001.10:g.27105698G>T , CM000663.1:g.27105698G>T	GRCh37
NC_000001.9:g.26978285G>T	NCBI36
NG_029965.1:g.88177G>T , LRG_875:g.88177G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5309G>T MANE Select	ENSP00000320485.7:p.Gly1770Val
ENST00000374152.7:c.4160G>T	ENSP00000363267.2:p.Gly1387Val
ENST00000430799.7:c.4157G>T	ENSP00000390317.3:p.Gly1386Val
ENST00000466382.2:c.726G>T
ENST00000636219.1:c.4163G>T	ENSP00000489842.1:p.Gly1388Val
ENST00000637788.1:n.1109G>T
ENST00000324856.11:c.5309G>T	ENSP00000320485.7:p.Gly1770Val
ENST00000374152.6:c.4160G>T	ENSP00000363267.2:p.Gly1387Val
ENST00000430799.6:c.1998G>T
ENST00000457599.6:c.4658G>T	ENSP00000387636.2:p.Gly1553Val
ENST00000466382.1:c.726G>T
ENST00000532781.1:c.807G>T
NM_006015.4:c.5309G>T , LRG_875t1:c.5309G>T	NP_006006.3:p.Gly1770Val
NM_139135.2:c.4658G>T	NP_624361.1:p.Gly1553Val
NM_006015.5:c.5309G>T	NP_006006.3:p.Gly1770Val
NM_139135.3:c.4658G>T	NP_624361.1:p.Gly1553Val
NM_006015.6:c.5309G>T MANE Select	NP_006006.3:p.Gly1770Val
NM_139135.4:c.4658G>T	NP_624361.1:p.Gly1553Val