Canonical Allele Identifier: CA412613864
Gene: ARX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.25033740A>C (hg19) chrX:g.25015623A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015623A>C , CM000685.2:g.25015623A>C GRCh38
NC_000023.10:g.25033740A>C , CM000685.1:g.25033740A>C GRCh37
NC_000023.9:g.24943661A>C NCBI36
NG_008281.1:g.5326T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.115T>G MANE Select ENSP00000368332.4:p.Cys39Gly
ENST00000636609.1:n.58T>G
ENST00000637394.1:n.90T>G
ENST00000379044.4:c.115T>G ENSP00000368332.4:p.Cys39Gly
NM_139058.2:c.115T>G NP_620689.1:p.Cys39Gly
NM_139058.3:c.115T>G MANE Select NP_620689.1:p.Cys39Gly
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Search 100 bp 3'