Linked Data
MyVariant Identifiers:
chrMT:g.4120T>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.4120T= , J01415.2:m.4120T= | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361390.2:c.814T= | ENSP00000354687.2:p.Ter272= |