Canonical Allele Identifier: CA414819219
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13720C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13720C>G , J01415.2:m.13720C>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1384C>G ENSP00000354813.2:p.Leu462Val