Canonical Allele Identifier: CA345705
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 140589
dbSNP Id: rs193302985
MyVariant Identifiers: chrMT:g.15043G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15043G>A , J01415.2:m.15043G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.297G>A ENSP00000354554.2:p.Gly99=