Canonical Allele Identifier: CA337100209
Gene: MT-CYB HGNC NCBI

Linked Data

dbSNP Id: rs386829229
MyVariant Identifiers: chrMT:g.14914A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14914A>C , J01415.2:m.14914A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.168A>C ENSP00000354554.2:p.Ser56=
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