Canonical Allele Identifier: CA337097668
Gene: MT-CO2 HGNC NCBI

Linked Data

dbSNP Id: rs386829011
MyVariant Identifiers: chrMT:g.7633C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7633C>A , J01415.2:m.7633C>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361739.1:c.48C>A ENSP00000354876.1:p.Ile16=
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