Canonical Allele Identifier: CA340946
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9729
dbSNP Id: rs28358582
MyVariant Identifiers: chrMT:g.3308T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3308T>G , J01415.2:m.3308T>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.2T>G ENSP00000354687.2:p.Ile1Arg