Canonical Allele Identifier: CA414812491
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.12099T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12099T>C , J01415.2:m.12099T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1340T>C ENSP00000354961.2:p.Leu447Pro