Canonical Allele Identifier: CA999839765
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs1190154028
gnomAD v3: 1-26696389-G-C
gnomAD v4: 1-26696389-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696389G>C , CM000663.2:g.26696389G>C GRCh38
NC_000001.10:g.27022880G>C , CM000663.1:g.27022880G>C GRCh37
NC_000001.9:g.26895467G>C NCBI36
NG_029965.1:g.5359G>C , LRG_875:g.5359G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.-15G>C MANE Select ENSP00000320485.7:n.-15G>C
ENST00000430799.7:c.-13+2772G>C ENSP00000390317.3:n.-13+2772G>C
ENST00000637465.1:c.-13+289G>C ENSP00000490650.1:n.-13+289G>C
ENST00000324856.11:c.-15G>C ENSP00000320485.7:n.-15G>C
NM_006015.4:c.-15G>C , LRG_875t1:c.-15G>C NP_006006.3:n.-15G>C
NM_139135.2:c.-15G>C NP_624361.1:n.-15G>C
XM_011542542.1:c.17C>G XP_011540844.1:p.Ser6Trp
NM_006015.5:c.-15G>C NP_006006.3:n.-15G>C
NM_139135.3:c.-15G>C NP_624361.1:n.-15G>C
NM_006015.6:c.-15G>C MANE Select NP_006006.3:n.-15G>C
NM_139135.4:c.-15G>C NP_624361.1:n.-15G>C