Canonical Allele Identifier: CA414809506
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693343
ClinVar RCV Id: RCV000854707
dbSNP Id: rs1603223116
MyVariant Identifiers: chrMT:g.11120T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11120T>C , J01415.2:m.11120T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.361T>C ENSP00000354961.2:p.Phe121Leu