Canonical Allele Identifier: CA414772518
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692331
ClinVar RCV Id: RCV000853631
dbSNP Id: rs1603218891
MyVariant Identifiers: chrMT:g.3313A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3313A>G , J01415.2:m.3313A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.7A>G ENSP00000354687.2:p.Met3Val