Canonical Allele Identifier: CA414804292
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693263
ClinVar RCV Id: RCV000854620
dbSNP Id: rs1603222676
MyVariant Identifiers: chrMT:g.10111T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10111T>C , J01415.2:m.10111T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.53T>C ENSP00000355206.2:p.Ile18Thr
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