Canonical Allele Identifier: CA414780619
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 585066
ClinVar RCV Id: RCV000709825 RCV000853916
dbSNP Id: rs1569484003
MyVariant Identifiers: chrMT:g.5505A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5505A>G , J01415.2:m.5505A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.1036A>G ENSP00000355046.4:p.Ile346Val
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