Canonical Allele Identifier: CA414818786
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13619T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13619T>A , J01415.2:m.13619T>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1283T>A ENSP00000354813.2:p.Leu428His