Canonical Allele Identifier: CA337097121
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs878980147
MyVariant Identifiers: chrMT:g.5378A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5378A>G , J01415.2:m.5378A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.909A>G ENSP00000355046.4:p.Thr303=
Search 100 bp 5'
Search 100 bp 3'