Canonical Allele Identifier: CA270616
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143890
ClinVar RCV Id: RCV000133429 RCV000855298
dbSNP Id: rs527236185
MyVariant Identifiers: chrMT:g.15458T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15458T>C , J01415.2:m.15458T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.712T>C ENSP00000354554.2:p.Ser238Pro
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