Canonical Allele Identifier: CA337097370
Gene: MT-CO1 HGNC NCBI

Linked Data

dbSNP Id: rs879224746
MyVariant Identifiers: chrMT:g.6293T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6293T>C , J01415.2:m.6293T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.390T>C ENSP00000354499.2:p.Pro130=