Linked Data
MyVariant Identifiers:
chrMT:g.11558T>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.11558T= , J01415.2:m.11558T= | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361381.2:c.799T= | ENSP00000354961.2:p.Ter267= |