Canonical Allele Identifier: CA414780609
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs1603219991
MyVariant Identifiers: chrMT:g.5503T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5503T>C , J01415.2:m.5503T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.1034T>C ENSP00000355046.4:p.Ile345Thr
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