Canonical Allele Identifier: CA120620
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9682
ClinVar RCV Id: RCV000010320
dbSNP Id: rs207460001
MyVariant Identifiers: chrMT:g.15197T>C (hg38)
PubMed: PMID:11464242
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15197T>C , J01415.2:m.15197T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.451T>C ENSP00000354554.2:p.Ser151Pro
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