Canonical Allele Identifier: CA2695678091
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs2124739653

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696402T>G , CM000663.2:g.26696402T>G GRCh38
NC_000001.10:g.27022893T>G , CM000663.1:g.27022893T>G GRCh37
NC_000001.9:g.26895480T>G NCBI36
NG_029965.1:g.5372T>G , LRG_875:g.5372T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.-2T>G MANE Select ENSP00000320485.7:n.-2T>G
ENST00000430799.7:c.-13+2785T>G ENSP00000390317.3:n.-13+2785T>G
ENST00000637465.1:c.-13+302T>G ENSP00000490650.1:n.-13+302T>G
ENST00000324856.11:c.-2T>G ENSP00000320485.7:n.-2T>G
NM_006015.4:c.-2T>G , LRG_875t1:c.-2T>G NP_006006.3:n.-2T>G
NM_139135.2:c.-2T>G NP_624361.1:n.-2T>G
XM_011542542.1:c.4A>C XP_011540844.1:p.Ile2Leu
NM_006015.5:c.-2T>G NP_006006.3:n.-2T>G
NM_139135.3:c.-2T>G NP_624361.1:n.-2T>G
NM_006015.6:c.-2T>G MANE Select NP_006006.3:n.-2T>G
NM_139135.4:c.-2T>G NP_624361.1:n.-2T>G