Canonical Allele Identifier: CA414819040
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13676A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13676A>T , J01415.2:m.13676A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1340A>T ENSP00000354813.2:p.Asn447Ile