Canonical Allele Identifier: CA270607
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143876
ClinVar RCV Id: RCV000133415 RCV002247523
dbSNP Id: rs527236173
MyVariant Identifiers: chrMT:g.15214T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15214T>C , J01415.2:m.15214T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.468T>C ENSP00000354554.2:p.Ile156=
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