Canonical Allele Identifier: CA120638
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 9713
ClinVar RCV Id: RCV000010359 RCV000854647
dbSNP Id: rs2853826
MyVariant Identifiers: chrMT:g.10398A>G (hg38)
PubMed: PMID:6343397 PMID:17066297
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10398A>G , J01415.2:m.10398A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.340A>G ENSP00000355206.2:p.Thr114Ala
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