Canonical Allele Identifier: CA414779590
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs1603219862
MyVariant Identifiers: chrMT:g.5269T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5269T>C , J01415.2:m.5269T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.800T>C ENSP00000355046.4:p.Ile267Thr