Canonical Allele Identifier: CA414812379
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693408
ClinVar RCV Id: RCV000854776
dbSNP Id: rs1603223534
MyVariant Identifiers: chrMT:g.12074A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12074A>C , J01415.2:m.12074A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1315A>C ENSP00000354961.2:p.Ile439Leu
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