Canonical Allele Identifier: CA10581386
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 235650
ClinVar RCV Id: RCV000224187
dbSNP Id: rs878853086
MyVariant Identifiers: chrMT:g.15514T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15514T>C , J01415.2:m.15514T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.768T>C ENSP00000354554.2:p.Tyr256=
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