Canonical Allele Identifier: CA515947626
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25013272-C-T
MyVariant Identifiers: chrX:g.25031389C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013272C>T , CM000685.2:g.25013272C>T GRCh38
NC_000023.10:g.25031389C>T , CM000685.1:g.25031389C>T GRCh37
NC_000023.9:g.24941310C>T NCBI36
NG_008281.1:g.7677G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.723G>A MANE Select ENSP00000368332.4:p.Glu241=
ENST00000379044.4:c.723G>A ENSP00000368332.4:p.Glu241=
NM_139058.2:c.723G>A NP_620689.1:p.Glu241=
NM_139058.3:c.723G>A MANE Select NP_620689.1:p.Glu241=