Canonical Allele Identifier: CA412611370

Gene: ARX

Linked Data

• dbSNP Id: rs1374295378
• gnomAD v2: X-25025408-T-C
• gnomAD v4: X-25007291-T-C
• MyVariant Identifiers: chrX:g.25025408T>C (hg19) ; chrX:g.25007291T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25007291T>C , CM000685.2:g.25007291T>C	GRCh38
NC_000023.10:g.25025408T>C , CM000685.1:g.25025408T>C	GRCh37
NC_000023.9:g.24935329T>C	NCBI36
NG_008281.1:g.13658A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379044.5:c.1268A>G MANE Select	ENSP00000368332.4:p.His423Arg
ENST00000379044.4:c.1268A>G	ENSP00000368332.4:p.His423Arg
NM_139058.2:c.1268A>G	NP_620689.1:p.His423Arg
NM_139058.3:c.1268A>G MANE Select	NP_620689.1:p.His423Arg