Canonical Allele Identifier: CA414775023
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs2124592314
MyVariant Identifiers: chrMT:g.4627C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4627C>T , J01415.2:m.4627C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.158C>T ENSP00000355046.4:p.Thr53Ile
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