ClinGen Allele Registry
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Canonical Allele Identifier:
CA10581349
Gene: MT-CO3
HGNC
NCBI
Linked Data
ClinVar Variation Id:
235541
ClinVar RCV Id:
RCV000224115
dbSNP Id:
rs386829076
MyVariant Identifiers:
chrMT:g.9368A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.9368A>G , J01415.2:m.9368A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000362079.2:c.162A>G
ENSP00000354982.2:p.Ile54Met
Search 100 bp 5'
Search 100 bp 3'