Canonical Allele Identifier: CA414812452
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.12090T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12090T>C , J01415.2:m.12090T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.1331T>C ENSP00000354961.2:p.Ile444Thr