Canonical Allele Identifier: CA337100383
Gene: MT-CYB HGNC NCBI

Linked Data

dbSNP Id: rs879239614
MyVariant Identifiers: chrMT:g.15391C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15391C>T , J01415.2:m.15391C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.645C>T ENSP00000354554.2:p.Ser215=
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