Canonical Allele Identifier: CA2644293898
Gene: ARID1A HGNC NCBI

Linked Data

gnomAD v4: 1-26696338-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696338G>C , CM000663.2:g.26696338G>C GRCh38
NC_000001.10:g.27022829G>C , CM000663.1:g.27022829G>C GRCh37
NC_000001.9:g.26895416G>C NCBI36
NG_029965.1:g.5308G>C , LRG_875:g.5308G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.-66G>C MANE Select ENSP00000320485.7:n.-66G>C
ENST00000430799.7:c.-13+2721G>C ENSP00000390317.3:n.-13+2721G>C
ENST00000637465.1:c.-13+238G>C ENSP00000490650.1:n.-13+238G>C
ENST00000324856.11:c.-66G>C ENSP00000320485.7:n.-66G>C
NM_006015.4:c.-66G>C , LRG_875t1:c.-66G>C NP_006006.3:n.-66G>C
NM_139135.2:c.-66G>C NP_624361.1:n.-66G>C
XM_011542542.1:c.45+23C>G XP_011540844.1:n.45+23C>G
NM_006015.5:c.-66G>C NP_006006.3:n.-66G>C
NM_139135.3:c.-66G>C NP_624361.1:n.-66G>C
NM_006015.6:c.-66G>C MANE Select NP_006006.3:n.-66G>C
NM_139135.4:c.-66G>C NP_624361.1:n.-66G>C