Canonical Allele Identifier: CA412610964
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25004902-G-T
MyVariant Identifiers: chrX:g.25023019G>T (hg19) chrX:g.25004902G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004902G>T , CM000685.2:g.25004902G>T GRCh38
NC_000023.10:g.25023019G>T , CM000685.1:g.25023019G>T GRCh37
NC_000023.9:g.24932940G>T NCBI36
NG_008281.1:g.16047C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1457C>A MANE Select ENSP00000368332.4:p.Ser486Tyr
ENST00000636885.1:n.45C>A
ENST00000379044.4:c.1457C>A ENSP00000368332.4:p.Ser486Tyr
NM_139058.2:c.1457C>A NP_620689.1:p.Ser486Tyr
NM_139058.3:c.1457C>A MANE Select NP_620689.1:p.Ser486Tyr
Search 100 bp 5'
Search 100 bp 3'