Canonical Allele Identifier: CA734489638

Gene: ARID1A

Linked Data

• dbSNP Id: rs1307454158
• gnomAD v3: 1-26696337-C-G
• gnomAD v4: 1-26696337-C-G
• MyVariant Identifiers: chr1:g.27022828C>G (hg19) ; chr1:g.26696337C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696337C>G , CM000663.2:g.26696337C>G	GRCh38
NC_000001.10:g.27022828C>G , CM000663.1:g.27022828C>G	GRCh37
NC_000001.9:g.26895415C>G	NCBI36
NG_029965.1:g.5307C>G , LRG_875:g.5307C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.-67C>G MANE Select	ENSP00000320485.7:n.-67C>G
ENST00000430799.7:c.-13+2720C>G	ENSP00000390317.3:n.-13+2720C>G
ENST00000637465.1:c.-13+237C>G	ENSP00000490650.1:n.-13+237C>G
ENST00000324856.11:c.-67C>G	ENSP00000320485.7:n.-67C>G
NM_006015.4:c.-67C>G , LRG_875t1:c.-67C>G	NP_006006.3:n.-67C>G
NM_139135.2:c.-67C>G	NP_624361.1:n.-67C>G
XM_011542542.1:c.45+24G>C	XP_011540844.1:n.45+24G>C
NM_006015.5:c.-67C>G	NP_006006.3:n.-67C>G
NM_139135.3:c.-67C>G	NP_624361.1:n.-67C>G
NM_006015.6:c.-67C>G MANE Select	NP_006006.3:n.-67C>G
NM_139135.4:c.-67C>G	NP_624361.1:n.-67C>G