Canonical Allele Identifier: CA999839675
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs1006487095
gnomAD v3: 1-26696342-T-C
gnomAD v4: 1-26696342-T-C

Genomic Alleles

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

Transcript Alleles

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