Canonical Allele Identifier: CA337100550
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693970
ClinVar RCV Id: RCV000855393
dbSNP Id: rs201023973
MyVariant Identifiers: chrMT:g.15860A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15860A>G , J01415.2:m.15860A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1114A>G ENSP00000354554.2:p.Ile372Val
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Search 100 bp 3'