Canonical Allele Identifier: CA414793436
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692766
ClinVar RCV Id: RCV000854093
dbSNP Id: rs1556423337
MyVariant Identifiers: chrMT:g.7718A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7718A>G , J01415.2:m.7718A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.133A>G ENSP00000354876.1:p.Thr45Ala
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