Canonical Allele Identifier: CA337096789
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692422
ClinVar RCV Id: RCV000853732
dbSNP Id: rs200180511
MyVariant Identifiers: chrMT:g.4093A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4093A>G , J01415.2:m.4093A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.787A>G ENSP00000354687.2:p.Thr263Ala