Canonical Allele Identifier: CA412612813
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25013387-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013387T>C , CM000685.2:g.25013387T>C GRCh38
NC_000023.10:g.25031504T>C , CM000685.1:g.25031504T>C GRCh37
NC_000023.9:g.24941425T>C NCBI36
NG_008281.1:g.7562A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.608A>G MANE Select ENSP00000368332.4:p.Glu203Gly
ENST00000379044.4:c.608A>G ENSP00000368332.4:p.Glu203Gly
NM_139058.2:c.608A>G NP_620689.1:p.Glu203Gly
NM_139058.3:c.608A>G MANE Select NP_620689.1:p.Glu203Gly