Canonical Allele Identifier: CA874141432
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs1409236687
MyVariant Identifiers: chrX:g.25022710T>C (hg19) chrX:g.25004593T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004593T>C , CM000685.2:g.25004593T>C GRCh38
NC_000023.10:g.25022710T>C , CM000685.1:g.25022710T>C GRCh37
NC_000023.9:g.24932631T>C NCBI36
NG_008281.1:g.16356A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.*77A>G MANE Select ENSP00000368332.4:n.*77A>G
ENST00000379044.4:c.*77A>G ENSP00000368332.4:n.*77A>G
NM_139058.2:c.*77A>G NP_620689.1:n.*77A>G
NM_139058.3:c.*77A>G MANE Select NP_620689.1:n.*77A>G
Search 100 bp 5'
Search 100 bp 3'