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Canonical Allele Identifier:
CA414780961
Gene: MT-CO1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.5949G>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.5949G>C , J01415.2:m.5949G>C
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361624.2:c.46G>C
ENSP00000354499.2:p.Gly16Arg
Search 100 bp 5'
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