Canonical Allele Identifier: CA10586049
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 252455
ClinVar RCV Id: RCV000238892 RCV000855396
dbSNP Id: rs527236195
MyVariant Identifiers: chrMT:g.15884G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15884G>C , J01415.2:m.15884G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1138G>C ENSP00000354554.2:p.Ala380Pro
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