Canonical Allele Identifier: CA10581430
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235783
ClinVar RCV Id: RCV000224370
dbSNP Id: rs7340122
MyVariant Identifiers: chrMT:g.5951A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5951A>G , J01415.2:m.5951A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361624.2:c.48A>G ENSP00000354499.2:p.Gly16=
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