Canonical Allele Identifier: CA337096932
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs28600732
MyVariant Identifiers: chrMT:g.4655G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4655G>A , J01415.2:m.4655G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.186G>A ENSP00000355046.4:p.Thr62=
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