Canonical Allele Identifier: CA414792193

Gene: MT-CO1

Linked Data

• ClinVar Variation Id: 692726
• ClinVar RCV Id: RCV000854051
• dbSNP Id: rs1556423264
• MyVariant Identifiers: chrMT:g.7278T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7278T>C , J01415.2:m.7278T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361624.2:c.1375T>C	ENSP00000354499.2:p.Phe459Leu