Canonical Allele Identifier: CA337097324
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 994643
ClinVar RCV Id: RCV001288244
dbSNP Id: rs879104796
MyVariant Identifiers: chrMT:g.6047A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6047A>G , J01415.2:m.6047A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.144A>G ENSP00000354499.2:p.Leu48=