Canonical Allele Identifier: CA913172083
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693763
ClinVar RCV Id: RCV000855154
dbSNP Id: rs1603224884
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14786A>G , J01415.2:m.14786A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.40A>G ENSP00000354554.2:p.Ile14Val
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