Humanin (HN): nomenclature notes
The humanin coding sequence lies within MT-RNR2, the mitochondrial 16S rRNA gene. A mitochondrial coding locus does not establish where translation occurs. This record specifies the 24-residue standard-code form; a mitochondrial-code prediction is a distinct sequence. Nuclear humanin-like loci further complicate assigning endogenous origin. HNG carries S14G, and HNGF6A carries F6A and S14G. N-formyl humanin is a distinct chemical form. MTRNR2L gene names denote nuclear loci and are not peptide aliases.
HNG ([Gly14]-Humanin): nomenclature notes
HNG, S14G-HN and [Gly14]-humanin name the same substitution. 'Humanin-G' denotes substitution at position 14, not a glycine extension. HNGF6A additionally replaces Phe6 with alanine. These synthetic analogs require sequence-specific attribution; mitochondrial family membership does not establish endogenous expression.