Linked Data
MyVariant Identifiers:
chrMT:g.5976T>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.5976T= , J01415.2:m.5976T= | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361624.2:c.73T= | ENSP00000354499.2:p.Ter25= |