Canonical Allele Identifier: CA414804289
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693262
ClinVar RCV Id: RCV000854619
dbSNP Id: rs1603222674
MyVariant Identifiers: chrMT:g.10110A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10110A>G , J01415.2:m.10110A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.52A>G ENSP00000355206.2:p.Ile18Val
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