ClinGen Allele Registry
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Canonical Allele Identifier:
CA337097545
Gene: MT-CO1
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.7055A>G
Linked Data - NCBI & NCI
dbSNP:
1978002
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.7055A>G , J01415.2:m.7055A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361624.2:c.1152A>G
ENSP00000354499.2:p.Gly384=
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