Canonical Allele Identifier: CA337097129
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs878971359
MyVariant Identifiers: chrMT:g.5402A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5402A>G , J01415.2:m.5402A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.933A>G ENSP00000355046.4:p.Val311=
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