Canonical Allele Identifier: CA337098646
Gene: MT-CO3 HGNC NCBI

Linked Data

dbSNP Id: rs879229894
MyVariant Identifiers: chrMT:g.9962G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9962G>A , J01415.2:m.9962G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000362079.2:c.756G>A ENSP00000354982.2:p.Leu252=