Canonical Allele Identifier: CA414819121
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13697T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13697T>A , J01415.2:m.13697T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1361T>A ENSP00000354813.2:p.Ile454Asn