Linked Data
MyVariant Identifiers:
chrMT:g.9952G>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9952G= , J01415.2:m.9952G= | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000362079.2:c.746G= | ENSP00000354982.2:p.Ter249= |