Canonical Allele Identifier: CA913172889
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693822
ClinVar RCV Id: RCV000855220
dbSNP Id: rs386829235
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15080A>G , J01415.2:m.15080A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.334A>G ENSP00000354554.2:p.Thr112Ala
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