Canonical Allele Identifier: CA414772535
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692334
ClinVar RCV Id: RCV000853634
dbSNP Id: rs1603218896
MyVariant Identifiers: chrMT:g.3320A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3320A>G , J01415.2:m.3320A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.14A>G ENSP00000354687.2:p.Asn5Ser