Canonical Allele Identifier: CA414781060
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692603
ClinVar RCV Id: RCV000853922
dbSNP Id: rs1556423059
MyVariant Identifiers: chrMT:g.5973G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5973G>A , J01415.2:m.5973G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.70G>A ENSP00000354499.2:p.Ala24Thr