Canonical Allele Identifier: CA913174106
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693900
ClinVar RCV Id: RCV000855316
dbSNP Id: rs1603225331

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15524A>G , J01415.2:m.15524A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.778A>G ENSP00000354554.2:p.Asn260Asp