Canonical Allele Identifier: CA16040639
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 370062
ClinVar RCV Id: RCV000408920 RCV000855214
dbSNP Id: rs1057516072
MyVariant Identifiers: chrMT:g.15060G>A (hg38)
PubMed: PMID:28027978
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15060G>A , J01415.2:m.15060G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.314G>A ENSP00000354554.2:p.Gly105Glu
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