Canonical Allele Identifier: CA337100548
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693966
ClinVar RCV Id: RCV000855389
dbSNP Id: rs3094281
MyVariant Identifiers: chrMT:g.15851A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15851A>G , J01415.2:m.15851A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1105A>G ENSP00000354554.2:p.Ile369Val