Canonical Allele Identifier: CA120618
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9680
ClinVar RCV Id: RCV000010318 RCV000855252
dbSNP Id: rs207459999
MyVariant Identifiers: chrMT:g.15242G>A (hg38)
PubMed: PMID:11047755
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15242G>A , J01415.2:m.15242G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.496G>A ENSP00000354554.2:p.Gly166Arg
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