Canonical Allele Identifier: CA337100466
Gene: MT-CYB HGNC NCBI

Linked Data

dbSNP Id: rs28357373
MyVariant Identifiers: chrMT:g.15629T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15629T>C , J01415.2:m.15629T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.883T>C ENSP00000354554.2:p.Leu295=