Canonical Allele Identifier: CA337099359
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693392
ClinVar RCV Id: RCV000854760
dbSNP Id: rs28359169
MyVariant Identifiers: chrMT:g.11969G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11969G>A , J01415.2:m.11969G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1210G>A ENSP00000354961.2:p.Ala404Thr
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