ClinGen Allele Registry
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Canonical Allele Identifier:
CA414791587
Gene: MT-CO1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1603220807
MyVariant Identifiers:
chrMT:g.7154A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.7154A>G , J01415.2:m.7154A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361624.2:c.1251A>G
ENSP00000354499.2:p.Ile417Met
Search 100 bp 5'
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