Canonical Allele Identifier: CA414793201
Gene: MT-CO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.7662A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7662A>C , J01415.2:m.7662A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.77A>C ENSP00000354876.1:p.His26Pro