Canonical Allele Identifier: CA337096921
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs374292687
MyVariant Identifiers: chrMT:g.4634T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4634T>C , J01415.2:m.4634T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.165T>C ENSP00000355046.4:p.Ala55=