ClinGen Allele Registry
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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'