Canonical Allele Identifier: CA414814485
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.12708C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12708C>A , J01415.2:m.12708C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.372C>A ENSP00000354813.2:p.Phe124Leu