Canonical Allele Identifier: CA120647
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9733
dbSNP Id: rs199476122
MyVariant Identifiers: chrMT:g.3697G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3697G>A , J01415.2:m.3697G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.391G>A ENSP00000354687.2:p.Gly131Ser