Canonical Allele Identifier: CA641364661
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs1363110443
gnomAD v2: X-25033646-G-A
gnomAD v4: X-25015529-G-A
MyVariant Identifiers: chrX:g.25033646G>A (hg19) chrX:g.25015529G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015529G>A , CM000685.2:g.25015529G>A GRCh38
NC_000023.10:g.25033646G>A , CM000685.1:g.25033646G>A GRCh37
NC_000023.9:g.24943567G>A NCBI36
NG_008281.1:g.5420C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.196+13C>T MANE Select ENSP00000368332.4:n.196+13C>T
ENST00000379044.4:c.196+13C>T ENSP00000368332.4:n.196+13C>T
NM_139058.2:c.196+13C>T NP_620689.1:n.196+13C>T
NM_139058.3:c.196+13C>T MANE Select NP_620689.1:n.196+13C>T
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