Canonical Allele Identifier: CA337100176
Gene: MT-CYB HGNC NCBI

Linked Data

dbSNP Id: rs879000658
MyVariant Identifiers: chrMT:g.14866C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14866C>T , J01415.2:m.14866C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.120C>T ENSP00000354554.2:p.Cys40=
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