Canonical Allele Identifier: CA345910
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 155880
dbSNP Id: rs587776433
MyVariant Identifiers: chrMT:g.3481G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3481G>A , J01415.2:m.3481G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.175G>A ENSP00000354687.2:p.Glu59Lys