Canonical Allele Identifier: CA414814940
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.12805T>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12805T= , J01415.2:m.12805T= GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.469T= ENSP00000354813.2:p.Ter157=