Canonical Allele Identifier: CA337097677

Gene: MT-CO2

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