Canonical Allele Identifier: CA270614
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143886
ClinVar RCV Id: RCV000133425
dbSNP Id: rs527236181
MyVariant Identifiers: chrMT:g.15355G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15355G>A , J01415.2:m.15355G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.609G>A ENSP00000354554.2:p.Thr203=
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