Canonical Allele Identifier: CA414802947
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693162
ClinVar RCV Id: RCV000854515
dbSNP Id: rs1603222309
MyVariant Identifiers: chrMT:g.9439G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9439G>A , J01415.2:m.9439G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.233G>A ENSP00000354982.2:p.Gly78Asp
Search 100 bp 5'
Search 100 bp 3'