Canonical Allele Identifier: CA414812463
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693412
ClinVar RCV Id: RCV000854780
dbSNP Id: rs1603223542
MyVariant Identifiers: chrMT:g.12092C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.1333C>T ENSP00000354961.2:p.Leu445Phe
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