Canonical Allele Identifier: CA734489722

Gene: ARID1A

Linked Data

• dbSNP Id: rs769457045
• gnomAD v3: 1-26696399-G-C
• gnomAD v4: 1-26696399-G-C
• MyVariant Identifiers: chr1:g.27022890G>C (hg19) ; chr1:g.26696399G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696399G>C , CM000663.2:g.26696399G>C	GRCh38
NC_000001.10:g.27022890G>C , CM000663.1:g.27022890G>C	GRCh37
NC_000001.9:g.26895477G>C	NCBI36
NG_029965.1:g.5369G>C , LRG_875:g.5369G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.-5G>C MANE Select	ENSP00000320485.7:n.-5G>C
ENST00000430799.7:c.-13+2782G>C	ENSP00000390317.3:n.-13+2782G>C
ENST00000637465.1:c.-13+299G>C	ENSP00000490650.1:n.-13+299G>C
ENST00000324856.11:c.-5G>C	ENSP00000320485.7:n.-5G>C
NM_006015.4:c.-5G>C , LRG_875t1:c.-5G>C	NP_006006.3:n.-5G>C
NM_139135.2:c.-5G>C	NP_624361.1:n.-5G>C
XM_011542542.1:c.7C>G	XP_011540844.1:p.Pro3Ala
NM_006015.5:c.-5G>C	NP_006006.3:n.-5G>C
NM_139135.3:c.-5G>C	NP_624361.1:n.-5G>C
NM_006015.6:c.-5G>C MANE Select	NP_006006.3:n.-5G>C
NM_139135.4:c.-5G>C	NP_624361.1:n.-5G>C