MyVariant.info:
GRCh38
chrMT:g.3936C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3936C>A , J01415.2:m.3936C>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361390.2:c.630C>A | ENSP00000354687.2:p.Gly210= |