Canonical Allele Identifier: CA337100531
Gene: MT-CYB HGNC NCBI

Linked Data

dbSNP Id: rs879063269
MyVariant Identifiers: chrMT:g.15790C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15790C>T , J01415.2:m.15790C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1044C>T ENSP00000354554.2:p.Thr348=