Canonical Allele Identifier: CA120604
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9658
ClinVar RCV Id: RCV000010294
dbSNP Id: rs199474825
MyVariant Identifiers: chrMT:g.7587T>C (hg38)
PubMed: PMID:10205264
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7587T>C , J01415.2:m.7587T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361739.1:c.2T>C ENSP00000354876.1:p.Met1Thr
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