Canonical Allele Identifier: CA414812599
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693414
ClinVar RCV Id: RCV000854782
dbSNP Id: rs1603223553
MyVariant Identifiers: chrMT:g.12122A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12122A>G , J01415.2:m.12122A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1363A>G ENSP00000354961.2:p.Thr455Ala
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