Canonical Allele Identifier: CA170529
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143893
ClinVar RCV Id: RCV000133432 RCV000223961
dbSNP Id: rs527236188
MyVariant Identifiers: chrMT:g.15511T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15511T>C , J01415.2:m.15511T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.765T>C ENSP00000354554.2:p.Asn255=
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