Canonical Allele Identifier: CA913174854
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693955
ClinVar RCV Id: RCV000855376
dbSNP Id: rs1603225497

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15793C>A , J01415.2:m.15793C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1047C>A ENSP00000354554.2:p.Ile349=