Linked Data
ClinVar Variation Id:
235619
ClinVar RCV Id:
RCV000224955
dbSNP Id:
rs878853081
MyVariant Identifiers:
chrMT:g.3849G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3849G>A , J01415.2:m.3849G>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361390.2:c.543G>A | ENSP00000354687.2:p.Leu181= |