Canonical Allele Identifier: CA515749959
Gene: ARX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.25033747C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015630C>T , CM000685.2:g.25015630C>T GRCh38
NC_000023.10:g.25033747C>T , CM000685.1:g.25033747C>T GRCh37
NC_000023.9:g.24943668C>T NCBI36
NG_008281.1:g.5319G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.108G>A MANE Select ENSP00000368332.4:p.Arg36=
ENST00000636609.1:n.51G>A
ENST00000637394.1:n.83G>A
ENST00000379044.4:c.108G>A ENSP00000368332.4:p.Arg36=
NM_139058.2:c.108G>A NP_620689.1:p.Arg36=
NM_139058.3:c.108G>A MANE Select NP_620689.1:p.Arg36=
Search 100 bp 5'
Search 100 bp 3'