Linked Data
MyVariant Identifiers:
chrMT:g.7321G>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.7321G= , J01415.2:m.7321G= | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361624.2:c.1418G= | ENSP00000354499.2:p.Ter473= |