Canonical Allele Identifier: CA414780387
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs1603219957
MyVariant Identifiers: chrMT:g.5446T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5446T>C , J01415.2:m.5446T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.977T>C ENSP00000355046.4:p.Leu326Pro