ClinGen Allele Registry
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Canonical Allele Identifier:
CA414804088
Gene: MT-CO3
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.9953A>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.9953A= , J01415.2:m.9953A=
GRCh38
Transcript Alleles
HGVS
Amino-acid change
ENST00000362079.2:c.747A=
ENSP00000354982.2:p.Ter249=
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