Canonical Allele Identifier: CA412612959

Gene: ARX

Linked Data

• dbSNP Id: rs1331739968
• gnomAD v2: X-25031576-C-A
• gnomAD v4: X-25013459-C-A
• MyVariant Identifiers: chrX:g.25031576C>A (hg19) ; chrX:g.25013459C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25013459C>A , CM000685.2:g.25013459C>A	GRCh38
NC_000023.10:g.25031576C>A , CM000685.1:g.25031576C>A	GRCh37
NC_000023.9:g.24941497C>A	NCBI36
NG_008281.1:g.7490G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379044.5:c.536G>T MANE Select	ENSP00000368332.4:p.Gly179Val
ENST00000379044.4:c.536G>T	ENSP00000368332.4:p.Gly179Val
NM_139058.2:c.536G>T	NP_620689.1:p.Gly179Val
NM_139058.3:c.536G>T MANE Select	NP_620689.1:p.Gly179Val