Canonical Allele Identifier: CA414775360
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692482
ClinVar RCV Id: RCV000853798
dbSNP Id: rs1603219566
MyVariant Identifiers: chrMT:g.4696T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4696T>C , J01415.2:m.4696T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.227T>C ENSP00000355046.4:p.Phe76Ser
Search 100 bp 5'
Search 100 bp 3'