ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA913173322
Gene: MT-CYB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
693851
ClinVar RCV Id:
RCV000855251
dbSNP Id:
rs1603225166
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.15238C>A , J01415.2:m.15238C>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361789.2:c.492C>A
ENSP00000354554.2:p.Ile164=
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