Canonical Allele Identifier: CA170521
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143874
dbSNP Id: rs527236171
MyVariant Identifiers: chrMT:g.15058C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15058C>T , J01415.2:m.15058C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.312C>T ENSP00000354554.2:p.Tyr104=