Canonical Allele Identifier: CA414793357
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692763
ClinVar RCV Id: RCV000854090
dbSNP Id: rs1603221090
MyVariant Identifiers: chrMT:g.7698T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7698T>C , J01415.2:m.7698T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.113T>C ENSP00000354876.1:p.Val38Ala
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Search 100 bp 3'