Canonical Allele Identifier: CA414774350
Gene: MT-ND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4176A>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4176A= , J01415.2:m.4176A= GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.870A= ENSP00000354687.2:p.Ter290=