Canonical Allele Identifier: CA337100501
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693939
ClinVar RCV Id: RCV000855357
dbSNP Id: rs879129589
MyVariant Identifiers: chrMT:g.15732C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15732C>T , J01415.2:m.15732C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.986C>T ENSP00000354554.2:p.Ala329Val
Search 100 bp 5'
Search 100 bp 3'