Canonical Allele Identifier: CA414793281
Gene: MT-CO2 HGNC NCBI

Linked Data

dbSNP Id: rs1603221080
MyVariant Identifiers: chrMT:g.7681C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7681C>A , J01415.2:m.7681C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.96C>A ENSP00000354876.1:p.Phe32Leu