ClinGen Allele Registry
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Canonical Allele Identifier:
CA414792996
Gene: MT-CO2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.7616G>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.7616G>A , J01415.2:m.7616G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361739.1:c.31G>A
ENSP00000354876.1:p.Asp11Asn
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