Canonical Allele Identifier: CA414810456
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.11559G>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11559G= , J01415.2:m.11559G= GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.800G= ENSP00000354961.2:p.Ter267=
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