Canonical Allele Identifier: CA120639
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 9714
dbSNP Id: rs199476117
MyVariant Identifiers: chrMT:g.10158T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10158T>C , J01415.2:m.10158T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.100T>C ENSP00000355206.2:p.Ser34Pro