Canonical Allele Identifier: CA414811200
Gene: MT-ND4 HGNC NCBI

Linked Data

dbSNP Id: rs1603223422
MyVariant Identifiers: chrMT:g.11814T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11814T>C , J01415.2:m.11814T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1055T>C ENSP00000354961.2:p.Leu352Pro