Canonical Allele Identifier: CA250587
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9676
dbSNP Id: rs207459995
MyVariant Identifiers: chrMT:g.14985G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14985G>A , J01415.2:m.14985G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:n.239G>A ENSP00000354554.2:p.Arg80His