Canonical Allele Identifier: CA414812583
Gene: MT-ND4 HGNC NCBI

Linked Data

dbSNP Id: rs1603223550
MyVariant Identifiers: chrMT:g.12119A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12119A>G , J01415.2:m.12119A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1360A>G ENSP00000354961.2:p.Ile454Val