Canonical Allele Identifier: CA913172884
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693821
ClinVar RCV Id: RCV000855219
dbSNP Id: rs1603225065
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15078A>G , J01415.2:m.15078A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.332A>G ENSP00000354554.2:p.Glu111Gly
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Search 100 bp 3'