Canonical Allele Identifier: CA913173767
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693877
ClinVar RCV Id: RCV000855284
dbSNP Id: rs200521299

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15401A>G , J01415.2:m.15401A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.655A>G ENSP00000354554.2:p.Thr219Ala