Canonical Allele Identifier: CA414793245
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692757
ClinVar RCV Id: RCV000854084
dbSNP Id: rs1569484167
MyVariant Identifiers: chrMT:g.7673A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7673A>G , J01415.2:m.7673A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.88A>G ENSP00000354876.1:p.Ile30Val
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