Canonical Allele Identifier: CA19668830
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs960676009
gnomAD v4: 1-26731108-A-G
MyVariant Identifiers: chr1:g.26731108A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26731108A>G , CM000663.2:g.26731108A>G GRCh38
NC_000001.10:g.27057599A>G , CM000663.1:g.27057599A>G GRCh37
NC_000001.9:g.26930186A>G NCBI36
NG_029965.1:g.40078A>G , LRG_875:g.40078A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.1351-44A>G MANE Select ENSP00000320485.7:n.1351-44A>G
ENST00000374152.7:c.202-44A>G ENSP00000363267.2:n.202-44A>G
ENST00000430799.7:c.202-44A>G ENSP00000390317.3:n.202-44A>G
ENST00000636219.1:c.208-44A>G ENSP00000489842.1:n.208-44A>G
ENST00000637465.1:c.202-44A>G ENSP00000490650.1:n.202-44A>G
ENST00000324856.11:c.1351-44A>G ENSP00000320485.7:n.1351-44A>G
ENST00000374152.6:c.202-44A>G ENSP00000363267.2:n.202-44A>G
ENST00000457599.6:c.1351-44A>G ENSP00000387636.2:n.1351-44A>G
ENST00000524572.1:c.202-44A>G ENSP00000432473.1:n.202-44A>G
ENST00000615191.4:c.202-44A>G ENSP00000478955.1:n.202-44A>G
NM_006015.4:c.1351-44A>G , LRG_875t1:c.1351-44A>G NP_006006.3:n.1351-44A>G
NM_139135.2:c.1351-44A>G NP_624361.1:n.1351-44A>G
NM_006015.5:c.1351-44A>G NP_006006.3:n.1351-44A>G
NM_139135.3:c.1351-44A>G NP_624361.1:n.1351-44A>G
NM_006015.6:c.1351-44A>G MANE Select NP_006006.3:n.1351-44A>G
NM_139135.4:c.1351-44A>G NP_624361.1:n.1351-44A>G