Canonical Allele Identifier: CA414815248
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.12869G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12869G>C , J01415.2:m.12869G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.533G>C ENSP00000354813.2:p.Gly178Ala