Canonical Allele Identifier: CA416989381

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124741061
• gnomAD v4: 1-26696670-C-G
• MyVariant Identifiers: chr1:g.27023161C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696670C>G , CM000663.2:g.26696670C>G	GRCh38
NC_000001.10:g.27023161C>G , CM000663.1:g.27023161C>G	GRCh37
NC_000001.9:g.26895748C>G	NCBI36
NG_029965.1:g.5640C>G , LRG_875:g.5640C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.267C>G MANE Select	ENSP00000320485.7:p.Gly89=
ENST00000430799.7:c.-13+3053C>G	ENSP00000390317.3:n.-13+3053C>G
ENST00000637465.1:c.-13+570C>G	ENSP00000490650.1:n.-13+570C>G
ENST00000324856.11:c.267C>G	ENSP00000320485.7:p.Gly89=
ENST00000457599.6:c.267C>G	ENSP00000387636.2:p.Gly89=
NM_006015.4:c.267C>G , LRG_875t1:c.267C>G	NP_006006.3:p.Gly89=
NM_139135.2:c.267C>G	NP_624361.1:p.Gly89=
NM_006015.5:c.267C>G	NP_006006.3:p.Gly89=
NM_139135.3:c.267C>G	NP_624361.1:p.Gly89=
NM_006015.6:c.267C>G MANE Select	NP_006006.3:p.Gly89=
NM_139135.4:c.267C>G	NP_624361.1:p.Gly89=