Canonical Allele Identifier: CA10581249
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235228
ClinVar RCV Id: RCV000224229
dbSNP Id: rs28357971
MyVariant Identifiers: chrMT:g.3843A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3843A>G , J01415.2:m.3843A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.537A>G ENSP00000354687.2:p.Ter179Trp