MyVariant.info:
GRCh38
chrMT:g.8655C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8655C>T , J01415.2:m.8655C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.129C>T | ENSP00000354632.2:p.Ile43= |