Canonical Allele Identifier: CA19640165

Gene: ARID1A

Linked Data

• dbSNP Id: rs1006487095
• gnomAD v2: 1-27022833-T-G
• gnomAD v3: 1-26696342-T-G
• gnomAD v4: 1-26696342-T-G
• MyVariant Identifiers: chr1:g.27022833T>G (hg19) ; chr1:g.26696342T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696342T>G , CM000663.2:g.26696342T>G	GRCh38
NC_000001.10:g.27022833T>G , CM000663.1:g.27022833T>G	GRCh37
NC_000001.9:g.26895420T>G	NCBI36
NG_029965.1:g.5312T>G , LRG_875:g.5312T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.-62T>G MANE Select	ENSP00000320485.7:n.-62T>G
ENST00000430799.7:c.-13+2725T>G	ENSP00000390317.3:n.-13+2725T>G
ENST00000637465.1:c.-13+242T>G	ENSP00000490650.1:n.-13+242T>G
ENST00000324856.11:c.-62T>G	ENSP00000320485.7:n.-62T>G
NM_006015.4:c.-62T>G , LRG_875t1:c.-62T>G	NP_006006.3:n.-62T>G
NM_139135.2:c.-62T>G	NP_624361.1:n.-62T>G
XM_011542542.1:c.45+19A>C	XP_011540844.1:n.45+19A>C
NM_006015.5:c.-62T>G	NP_006006.3:n.-62T>G
NM_139135.3:c.-62T>G	NP_624361.1:n.-62T>G
NM_006015.6:c.-62T>G MANE Select	NP_006006.3:n.-62T>G
NM_139135.4:c.-62T>G	NP_624361.1:n.-62T>G