Canonical Allele Identifier: CA345703
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 140587
dbSNP Id: rs193302980
MyVariant Identifiers: chrMT:g.14766C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14766C>T , J01415.2:m.14766C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.20C>T ENSP00000354554.2:p.Thr7Ile