Canonical Allele Identifier: CA270622
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143898
ClinVar RCV Id: RCV000133437 RCV000855365
dbSNP Id: rs527236193
MyVariant Identifiers: chrMT:g.15758A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15758A>G , J01415.2:m.15758A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1012A>G ENSP00000354554.2:p.Ile338Val
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