Canonical Allele Identifier: CA120610
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9665
ClinVar RCV Id: RCV000010303
dbSNP Id: rs199476127
MyVariant Identifiers: chrMT:g.6721T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6721T>C , J01415.2:m.6721T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.818T>C ENSP00000354499.2:p.Met273Thr