Canonical Allele Identifier: CA339264937

Gene: ARID1A

Linked Data

• dbSNP Id: rs2080260036
• gnomAD v4: 1-26696755-A-G
• MyVariant Identifiers: chr1:g.27023246A>G (hg19) ; chr1:g.26696755A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696755A>G , CM000663.2:g.26696755A>G	GRCh38
NC_000001.10:g.27023246A>G , CM000663.1:g.27023246A>G	GRCh37
NC_000001.9:g.26895833A>G	NCBI36
NG_029965.1:g.5725A>G , LRG_875:g.5725A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.352A>G MANE Select	ENSP00000320485.7:p.Thr118Ala
ENST00000430799.7:c.-13+3138A>G	ENSP00000390317.3:n.-13+3138A>G
ENST00000637465.1:c.-13+655A>G	ENSP00000490650.1:n.-13+655A>G
ENST00000324856.11:c.352A>G	ENSP00000320485.7:p.Thr118Ala
ENST00000457599.6:c.352A>G	ENSP00000387636.2:p.Thr118Ala
NM_006015.4:c.352A>G , LRG_875t1:c.352A>G	NP_006006.3:p.Thr118Ala
NM_139135.2:c.352A>G	NP_624361.1:p.Thr118Ala
NM_006015.5:c.352A>G	NP_006006.3:p.Thr118Ala
NM_139135.3:c.352A>G	NP_624361.1:p.Thr118Ala
NM_006015.6:c.352A>G MANE Select	NP_006006.3:p.Thr118Ala
NM_139135.4:c.352A>G	NP_624361.1:p.Thr118Ala