Canonical Allele Identifier: CA414795629
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692827
ClinVar RCV Id: RCV000854155
dbSNP Id: rs1603221342
MyVariant Identifiers: chrMT:g.8237A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8237A>G , J01415.2:m.8237A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.652A>G ENSP00000354876.1:p.Ile218Val
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