Canonical Allele Identifier: CA414811646
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693384
ClinVar RCV Id: RCV000854752
dbSNP Id: rs1603223463
MyVariant Identifiers: chrMT:g.11913C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11913C>T , J01415.2:m.11913C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.1154C>T ENSP00000354961.2:p.Thr385Met