Canonical Allele Identifier: CA414791420
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692702
ClinVar RCV Id: RCV000854027
dbSNP Id: rs1603220788
MyVariant Identifiers: chrMT:g.7129A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7129A>G , J01415.2:m.7129A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361624.2:c.1226A>G ENSP00000354499.2:p.Tyr409Cys