Canonical Allele Identifier: CA337097693
Gene: MT-CO2 HGNC NCBI

Linked Data

dbSNP Id: rs878875354
MyVariant Identifiers: chrMT:g.7738T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7738T>C , J01415.2:m.7738T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361739.1:c.153T>C ENSP00000354876.1:p.Thr51=