Canonical Allele Identifier: CA414819249
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13726G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13726G>C , J01415.2:m.13726G>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1390G>C ENSP00000354813.2:p.Ala464Pro