Canonical Allele Identifier: CA414793569
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692769
ClinVar RCV Id: RCV000854096
dbSNP Id: rs1603221115
MyVariant Identifiers: chrMT:g.7751T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7751T>G , J01415.2:m.7751T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.166T>G ENSP00000354876.1:p.Ser56Ala
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