Canonical Allele Identifier: CA209987
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 210337
ClinVar RCV Id: RCV000195280 RCV001425507
dbSNP Id: rs797045305
MyVariant Identifiers: chrX:g.25031365C>T (hg19) chrX:g.25013248C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013248C>T , CM000685.2:g.25013248C>T GRCh38
NC_000023.10:g.25031365C>T , CM000685.1:g.25031365C>T GRCh37
NC_000023.9:g.24941286C>T NCBI36
NG_008281.1:g.7701G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.747G>A MANE Select ENSP00000368332.4:p.Glu249=
ENST00000379044.4:c.747G>A ENSP00000368332.4:p.Glu249=
NM_139058.2:c.747G>A NP_620689.1:p.Glu249=
NM_139058.3:c.747G>A MANE Select NP_620689.1:p.Glu249=
Search 100 bp 5'
Search 100 bp 3'