ClinGen Allele Registry
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Canonical Allele Identifier:
CA414802756
Gene: MT-CO3
HGNC
NCBI
Linked Data
ClinVar Variation Id:
523307
ClinVar RCV Id:
RCV000626563
RCV000626562
dbSNP Id:
rs1556423663
MyVariant Identifiers:
chrMT:g.9355A>T (hg38)
JSON-LD
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
Search 100 bp 5'
Search 100 bp 3'