Linked Data
MyVariant Identifiers:
chrMT:g.12653G>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12653G= , J01415.2:m.12653G= | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361567.2:c.317G= | ENSP00000354813.2:p.Ter106= |