Canonical Allele Identifier: CA250583
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9659
dbSNP Id: rs199474826
MyVariant Identifiers: chrMT:g.8009G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8009G>A , J01415.2:m.8009G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361739.1:c.424G>A ENSP00000354876.1:p.Val142Ile