Canonical Allele Identifier: CA515749724
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 2121860
ClinVar RCV Id: RCV003049370
dbSNP Id: rs1390944438
gnomAD v2: X-25033660-T-C
gnomAD v4: X-25015543-T-C
MyVariant Identifiers: chrX:g.25033660T>C (hg19) chrX:g.25015543T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015543T>C , CM000685.2:g.25015543T>C GRCh38
NC_000023.10:g.25033660T>C , CM000685.1:g.25033660T>C GRCh37
NC_000023.9:g.24943581T>C NCBI36
NG_008281.1:g.5406A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.195A>G MANE Select ENSP00000368332.4:p.Gln65=
ENST00000379044.4:c.195A>G ENSP00000368332.4:p.Gln65=
NM_139058.2:c.195A>G NP_620689.1:p.Gln65=
NM_139058.3:c.195A>G MANE Select NP_620689.1:p.Gln65=
Search 100 bp 5'
Search 100 bp 3'