Canonical Allele Identifier: CA515748651
Gene: ARX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.25028383T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010266T>C , CM000685.2:g.25010266T>C GRCh38
NC_000023.10:g.25028383T>C , CM000685.1:g.25028383T>C GRCh37
NC_000023.9:g.24938304T>C NCBI36
NG_008281.1:g.10683A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.4:c.1113A>G ENSP00000368332.4:p.Arg371=
NM_139058.2:c.1113A>G NP_620689.1:p.Arg371=
NM_139058.3:c.1113A>G MANE Select NP_620689.1:p.Arg371=