Canonical Allele Identifier: CA412611003
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 812667
ClinVar RCV Id: RCV001003472
dbSNP Id: rs1468724042
gnomAD v2: X-25025232-C-T
gnomAD v4: X-25007115-C-T
MyVariant Identifiers: chrX:g.25025232C>T (hg19) chrX:g.25007115C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007115C>T , CM000685.2:g.25007115C>T GRCh38
NC_000023.10:g.25025232C>T , CM000685.1:g.25025232C>T GRCh37
NC_000023.9:g.24935153C>T NCBI36
NG_008281.1:g.13834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1444G>A MANE Select ENSP00000368332.4:p.Gly482Ser
ENST00000637993.1:c.57G>A
ENST00000379044.4:c.1444G>A ENSP00000368332.4:p.Gly482Ser
NM_139058.2:c.1444G>A NP_620689.1:p.Gly482Ser
NM_139058.3:c.1444G>A MANE Select NP_620689.1:p.Gly482Ser
Search 100 bp 5'
Search 100 bp 3'