Canonical Allele Identifier: CA2693353264
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25012807-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012807G>A , CM000685.2:g.25012807G>A GRCh38
NC_000023.10:g.25030924G>A , CM000685.1:g.25030924G>A GRCh37
NC_000023.9:g.24940845G>A NCBI36
NG_008281.1:g.8142C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1073+115C>T MANE Select ENSP00000368332.4:n.1073+115C>T
ENST00000379044.4:c.1073+115C>T ENSP00000368332.4:n.1073+115C>T
NM_139058.2:c.1073+115C>T NP_620689.1:n.1073+115C>T
NM_139058.3:c.1073+115C>T MANE Select NP_620689.1:n.1073+115C>T