Canonical Allele Identifier: CA412612778
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25013369-C-T
MyVariant Identifiers: chrX:g.25031486C>T (hg19) chrX:g.25013369C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013369C>T , CM000685.2:g.25013369C>T GRCh38
NC_000023.10:g.25031486C>T , CM000685.1:g.25031486C>T GRCh37
NC_000023.9:g.24941407C>T NCBI36
NG_008281.1:g.7580G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.626G>A MANE Select ENSP00000368332.4:p.Gly209Asp
ENST00000379044.4:c.626G>A ENSP00000368332.4:p.Gly209Asp
NM_139058.2:c.626G>A NP_620689.1:p.Gly209Asp
NM_139058.3:c.626G>A MANE Select NP_620689.1:p.Gly209Asp
Search 100 bp 5'
Search 100 bp 3'