Canonical Allele Identifier: CA120613
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9669
dbSNP Id: rs199476129
MyVariant Identifiers: chrMT:g.5920G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5920G>A , J01415.2:m.5920G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.17G>A ENSP00000354499.2:p.Ter6=