Canonical Allele Identifier: CA414811801
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693388
ClinVar RCV Id: RCV000854756
dbSNP Id: rs1603223482
MyVariant Identifiers: chrMT:g.11946C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11946C>T , J01415.2:m.11946C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1187C>T ENSP00000354961.2:p.Thr396Ile
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