Canonical Allele Identifier: CA337100269
Gene: MT-CYB HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.15080A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15080A>T , J01415.2:m.15080A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.334A>T ENSP00000354554.2:p.Thr112Ser