Linked Data
MyVariant Identifiers:
chrMT:g.9072A>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9072A>C , J01415.2:m.9072A>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.546A>C | ENSP00000354632.2:p.Ser182= |