Canonical Allele Identifier: CA414807568
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 618728
ClinVar RCV Id: RCV000757487 RCV000854693
dbSNP Id: rs1569484408
MyVariant Identifiers: chrMT:g.10931T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10931T>C , J01415.2:m.10931T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.172T>C ENSP00000354961.2:p.Ser58Pro
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