Canonical Allele Identifier: CA414802756
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 523307
dbSNP Id: rs1556423663
MyVariant Identifiers: chrMT:g.9355A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9355A>T , J01415.2:m.9355A>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000362079.2:c.149A>T ENSP00000354982.2:p.Asn50Ile