Canonical Allele Identifier: CA414775398
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs2068690024
MyVariant Identifiers: chrMT:g.4704A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4704A>C , J01415.2:m.4704A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.235A>C ENSP00000355046.4:p.Ile79Leu
Search 100 bp 5'
Search 100 bp 3'