Canonical Allele Identifier: CA414804297
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693264
ClinVar RCV Id: RCV000854621
dbSNP Id: rs1603222679
MyVariant Identifiers: chrMT:g.10113A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10113A>G , J01415.2:m.10113A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.55A>G ENSP00000355206.2:p.Ile19Val
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