Canonical Allele Identifier: CA250588
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9677
ClinVar RCV Id: RCV000010315
dbSNP Id: rs207459996
MyVariant Identifiers: chrMT:g.15572T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15572T>C , J01415.2:m.15572T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:n.826T>C ENSP00000354554.2:p.Phe276Leu