Canonical Allele Identifier: CA414780290
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs1603219941
MyVariant Identifiers: chrMT:g.5424C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5424C>T , J01415.2:m.5424C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.955C>T ENSP00000355046.4:p.His319Tyr
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