Canonical Allele Identifier: CA337099365
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3027422
ClinVar RCV Id: RCV003887815
dbSNP Id: rs2853497
MyVariant Identifiers: chrMT:g.12007G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12007G>A , J01415.2:m.12007G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1248G>A ENSP00000354961.2:p.Trp416Ter
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