Canonical Allele Identifier: CA414807483
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693325
ClinVar RCV Id: RCV000854687
dbSNP Id: rs1603223016
COSMIC: COSM488728
MyVariant Identifiers: chrMT:g.10911G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10911G>A , J01415.2:m.10911G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.152G>A ENSP00000354961.2:p.Ser51Asn
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Search 100 bp 3'