Canonical Allele Identifier: CA414790785
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692693
ClinVar RCV Id: RCV000854017
dbSNP Id: rs1603220739
MyVariant Identifiers: chrMT:g.7032T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7032T>C , J01415.2:m.7032T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361624.2:c.1129T>C ENSP00000354499.2:p.Phe377Leu