Canonical Allele Identifier: CA1160180533
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs1570537891
gnomAD v4: 1-26696374-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696374G>C , CM000663.2:g.26696374G>C GRCh38
NC_000001.10:g.27022865G>C , CM000663.1:g.27022865G>C GRCh37
NC_000001.9:g.26895452G>C NCBI36
NG_029965.1:g.5344G>C , LRG_875:g.5344G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.-30G>C MANE Select ENSP00000320485.7:n.-30G>C
ENST00000430799.7:c.-13+2757G>C ENSP00000390317.3:n.-13+2757G>C
ENST00000637465.1:c.-13+274G>C ENSP00000490650.1:n.-13+274G>C
ENST00000324856.11:c.-30G>C ENSP00000320485.7:n.-30G>C
NM_006015.4:c.-30G>C , LRG_875t1:c.-30G>C NP_006006.3:n.-30G>C
NM_139135.2:c.-30G>C NP_624361.1:n.-30G>C
XM_011542542.1:c.32C>G XP_011540844.1:p.Pro11Arg
NM_006015.5:c.-30G>C NP_006006.3:n.-30G>C
NM_139135.3:c.-30G>C NP_624361.1:n.-30G>C
NM_006015.6:c.-30G>C MANE Select NP_006006.3:n.-30G>C
NM_139135.4:c.-30G>C NP_624361.1:n.-30G>C