Canonical Allele Identifier: CA337096664
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692395
ClinVar RCV Id: RCV000853701
dbSNP Id: rs199684756
MyVariant Identifiers: chrMT:g.3746C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3746C>T , J01415.2:m.3746C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.440C>T ENSP00000354687.2:p.Ala147Val