Canonical Allele Identifier: CA337096717
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 805048
ClinVar RCV Id: RCV000992364
dbSNP Id: rs41524046
MyVariant Identifiers: chrMT:g.3915G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3915G>A , J01415.2:m.3915G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.609G>A ENSP00000354687.2:p.Gly203=