Canonical Allele Identifier: CA10581389
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 235655
ClinVar RCV Id: RCV000224926
dbSNP Id: rs28357683
MyVariant Identifiers: chrMT:g.14911C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14911C>T , J01415.2:m.14911C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.165C>T ENSP00000354554.2:p.Tyr55=
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