Linked Data
MyVariant Identifiers:
chrMT:g.7252G>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.7252G= , J01415.2:m.7252G= | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361624.2:c.1349G= | ENSP00000354499.2:p.Ter450= |