Canonical Allele Identifier: CA414773197
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692380
ClinVar RCV Id: RCV000853686
dbSNP Id: rs1603219059
MyVariant Identifiers: chrMT:g.3640G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3640G>A , J01415.2:m.3640G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.334G>A ENSP00000354687.2:p.Ala112Thr