Canonical Allele Identifier: CA16040652
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 370052
ClinVar RCV Id: RCV000408945 RCV002248640
dbSNP Id: rs1057516064
MyVariant Identifiers: chrMT:g.9237G>A (hg38)
PubMed: PMID:28027978
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9237G>A , J01415.2:m.9237G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000362079.2:c.31G>A ENSP00000354982.2:p.Val11Ile
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