Canonical Allele Identifier: CA1131754359
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs186187643
gnomAD v3: X-25004589-C-G
gnomAD v4: X-25004589-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004589C>G , CM000685.2:g.25004589C>G GRCh38
NC_000023.10:g.25022706C>G , CM000685.1:g.25022706C>G GRCh37
NC_000023.9:g.24932627C>G NCBI36
NG_008281.1:g.16360G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.*81G>C MANE Select ENSP00000368332.4:n.*81G>C
ENST00000379044.4:c.*81G>C ENSP00000368332.4:n.*81G>C
NM_139058.2:c.*81G>C NP_620689.1:n.*81G>C
NM_139058.3:c.*81G>C MANE Select NP_620689.1:n.*81G>C
Search 100 bp 5'
Search 100 bp 3'