Canonical Allele Identifier: CA414803267
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693187
ClinVar RCV Id: RCV000854540
dbSNP Id: rs1603222385
MyVariant Identifiers: chrMT:g.9588G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9588G>A , J01415.2:m.9588G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.382G>A ENSP00000354982.2:p.Glu128Lys
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Search 100 bp 3'