Canonical Allele Identifier: CA414803408
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693198
ClinVar RCV Id: RCV000854551
dbSNP Id: rs1603222415
MyVariant Identifiers: chrMT:g.9652A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9652A>G , J01415.2:m.9652A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.446A>G ENSP00000354982.2:p.His149Arg
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