Canonical Allele Identifier: CA645509242
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 374216
ClinVar RCV Id: RCV000509010
dbSNP Id: rs1556424489
MyVariant Identifiers: chrMT:g.14771C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14771C>A , J01415.2:m.14771C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.25C>A ENSP00000354554.2:p.Pro9Thr