Canonical Allele Identifier: CA344825
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 65515
ClinVar RCV Id: RCV000055703 RCV002260604
dbSNP Id: rs397515506
MyVariant Identifiers: chrMT:g.14568C>T (hg38)
ERepo: CA344825/MONDO:0044970/014
PubMed: PMID:20301353
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14568C>T , J01415.2:m.14568C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361681.2:c.106G>A ENSP00000354665.2:p.Gly36Ser
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