Canonical Allele Identifier: CA913173322
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693851
ClinVar RCV Id: RCV000855251
dbSNP Id: rs1603225166

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15238C>A , J01415.2:m.15238C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.492C>A ENSP00000354554.2:p.Ile164=