Canonical Allele Identifier: CA414803369
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693197
ClinVar RCV Id: RCV000854550
dbSNP Id: rs1603222412
MyVariant Identifiers: chrMT:g.9637T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9637T>C , J01415.2:m.9637T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.431T>C ENSP00000354982.2:p.Ile144Thr
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