Canonical Allele Identifier: CA414774832
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs1603219519
MyVariant Identifiers: chrMT:g.4587T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4587T>C , J01415.2:m.4587T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.118T>C ENSP00000355046.4:p.Phe40Leu
Search 100 bp 5'
Search 100 bp 3'