Canonical Allele Identifier: CA337097127
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs28631235
MyVariant Identifiers: chrMT:g.5399C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5399C>A , J01415.2:m.5399C>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.930C>A ENSP00000355046.4:p.Asn310Lys
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