Canonical Allele Identifier: CA412611714
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010264A>C , CM000685.2:g.25010264A>C GRCh38
NC_000023.10:g.25028381A>C , CM000685.1:g.25028381A>C GRCh37
NC_000023.9:g.24938302A>C NCBI36
NG_008281.1:g.10685T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.4:c.1115T>G ENSP00000368332.4:p.Val372Gly
NM_139058.2:c.1115T>G NP_620689.1:p.Val372Gly
NM_139058.3:c.1115T>G MANE Select NP_620689.1:p.Val372Gly