Canonical Allele Identifier: CA254852
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9675
ClinVar RCV Id: RCV000010313 RCV000855379
dbSNP Id: rs200336777
MyVariant Identifiers: chrMT:g.15812G>A (hg38)
PubMed: PMID:1732158 PMID:1764087
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15812G>A , J01415.2:m.15812G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1066G>A ENSP00000354554.2:p.Val356Ile
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