Canonical Allele Identifier: CA414783119
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692638
ClinVar RCV Id: RCV000853960
dbSNP Id: rs1603220406
MyVariant Identifiers: chrMT:g.6307A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6307A>G , J01415.2:m.6307A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.404A>G ENSP00000354499.2:p.Asn135Ser
Search 100 bp 5'
Search 100 bp 3'