Canonical Allele Identifier: CA120616
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9678
ClinVar RCV Id: RCV000010316 RCV000855331
dbSNP Id: rs207459997
MyVariant Identifiers: chrMT:g.15615G>A (hg38)
PubMed: PMID:8186719 PMID:8910895 PMID:10502593
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15615G>A , J01415.2:m.15615G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.869G>A ENSP00000354554.2:p.Gly290Asp
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