Canonical Allele Identifier: CA414811632
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.11910C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11910C>G , J01415.2:m.11910C>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.1151C>G ENSP00000354961.2:p.Thr384Ser