Canonical Allele Identifier: CA337097677
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692759
ClinVar RCV Id: RCV000854086
dbSNP Id: rs879003775
MyVariant Identifiers: chrMT:g.7679T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7679T>C , J01415.2:m.7679T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.94T>C ENSP00000354876.1:p.Phe32Leu