Canonical Allele Identifier: CA120623
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 9685
dbSNP Id: rs207460004
MyVariant Identifiers: chrMT:g.14849T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14849T>C , J01415.2:m.14849T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.103T>C ENSP00000354554.2:p.Ser35Pro