Canonical Allele Identifier: CA414811696
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.11923A>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11923A= , J01415.2:m.11923A= GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1164A= ENSP00000354961.2:p.Ter388=