Canonical Allele Identifier: CA414818792
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13621C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13621C>A , J01415.2:m.13621C>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1285C>A ENSP00000354813.2:p.Leu429Ile