Canonical Allele Identifier: CA337097689
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692762
ClinVar RCV Id: RCV000854089
dbSNP Id: rs879212765
MyVariant Identifiers: chrMT:g.7697G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7697G>A , J01415.2:m.7697G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.112G>A ENSP00000354876.1:p.Val38Ile
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