Canonical Allele Identifier: CA515947582
Gene: ARX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.25031311A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013194A>G , CM000685.2:g.25013194A>G GRCh38
NC_000023.10:g.25031311A>G , CM000685.1:g.25031311A>G GRCh37
NC_000023.9:g.24941232A>G NCBI36
NG_008281.1:g.7755T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.801T>C MANE Select ENSP00000368332.4:p.Pro267=
ENST00000379044.4:c.801T>C ENSP00000368332.4:p.Pro267=
NM_139058.2:c.801T>C NP_620689.1:p.Pro267=
NM_139058.3:c.801T>C MANE Select NP_620689.1:p.Pro267=
Search 100 bp 5'
Search 100 bp 3'