Canonical Allele Identifier: CA414821595
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693697
ClinVar RCV Id: RCV000855077
dbSNP Id: rs1556424407
MyVariant Identifiers: chrMT:g.14249G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14249G>A , J01415.2:m.14249G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.425C>T ENSP00000354665.2:p.Ala142Val
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