Canonical Allele Identifier: CA337100457
Gene: MT-CYB HGNC NCBI

Linked Data

dbSNP Id: rs386829253
MyVariant Identifiers: chrMT:g.15616C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15616C>T , J01415.2:m.15616C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.870C>T ENSP00000354554.2:p.Gly290=
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