Filtering for SNPCompendiumID: [1354884]

DNA Marker Index information for Chromosome: M Marker: H1cg
Names and Aliases for this DNA Marker: H1cg, H1aaa2.
Chromosome Position in hg38 Human Genome assembly1: 4767.
Chromosome Position in hg19 assembly2: 4767 .
Ancestral marker allele value: A.
Derived, alternative, or mutated marker allele value: G.


DNA Marker Index data SNPCompendiumID: 1354884
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
H1cg H1aaa2
 Major Haplogroup: H.
Phylogenetic branch with SNPs: A4767G. Example is GenBank accession JX153703.1 from Denmark. Formerly labeled H1-b1a1a and H1-b2.
DNA lineage H1cg is estimated to have originated in about the year 15,200 bce based on its position in the phylogenetic tree.
Phylogenetic Parent: H1aaa 
View Ancestry 		 PhyloTree.org
A
G
M
 4767
4767

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