Canonical Allele Identifier: CA414795635
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692828
ClinVar RCV Id: RCV000854156
dbSNP Id: rs1603221344
MyVariant Identifiers: chrMT:g.8238T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8238T>C , J01415.2:m.8238T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.653T>C ENSP00000354876.1:p.Ile218Thr
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