Canonical Allele Identifier: CA414792089
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.7252G>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7252G= , J01415.2:m.7252G= GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.1349G= ENSP00000354499.2:p.Ter450=
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