Canonical Allele Identifier: CA270602
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143869
dbSNP Id: rs527236166
MyVariant Identifiers: chrMT:g.14950C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14950C>T , J01415.2:m.14950C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.204C>T ENSP00000354554.2:p.His68=