ClinGen Allele Registry
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Canonical Allele Identifier:
CA414793377
Gene: MT-CO2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.7704A>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.7704A>G , J01415.2:m.7704A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361739.1:c.119A>G
ENSP00000354876.1:p.Tyr40Cys
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