Canonical Allele Identifier: CA414784832
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692661
ClinVar RCV Id: RCV000853985
dbSNP Id: rs386828988
MyVariant Identifiers: chrMT:g.6570G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6570G>T , J01415.2:m.6570G>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.667G>T ENSP00000354499.2:p.Ala223Ser
Search 100 bp 5'
Search 100 bp 3'