Canonical Allele Identifier: CA913172005
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693757
ClinVar RCV Id: RCV000855147
dbSNP Id: rs1603224859
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14757T>C , J01415.2:m.14757T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.11T>C ENSP00000354554.2:p.Ile4Thr
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