Canonical Allele Identifier: CA913172014
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693758
ClinVar RCV Id: RCV000855148
dbSNP Id: rs1603224860
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14760G>A , J01415.2:m.14760G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.14G>A ENSP00000354554.2:p.Arg5His
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