Canonical Allele Identifier: CA414793330

Gene: MT-CO2

Linked Data

• ClinVar Variation Id: 692761
• ClinVar RCV Id: RCV000854088
• dbSNP Id: rs1603221084
• MyVariant Identifiers: chrMT:g.7691T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7691T>C , J01415.2:m.7691T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361739.1:c.106T>C	ENSP00000354876.1:p.Phe36Leu