Canonical Allele Identifier: CA269988
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 140590
ClinVar RCV Id: RCV000128805 RCV000855263
dbSNP Id: rs527236044
MyVariant Identifiers: chrMT:g.15287T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15287T>C , J01415.2:m.15287T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.541T>C ENSP00000354554.2:p.Phe181Leu
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