Canonical Allele Identifier: CA414812460
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693411
ClinVar RCV Id: RCV000854779
dbSNP Id: rs1603223542
MyVariant Identifiers: chrMT:g.12092C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12092C>A , J01415.2:m.12092C>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.1333C>A ENSP00000354961.2:p.Leu445Ile
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