Canonical Allele Identifier: CA414823302
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693747
ClinVar RCV Id: RCV000855136
dbSNP Id: rs1556424471
MyVariant Identifiers: chrMT:g.14619A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14619A>G , J01415.2:m.14619A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.55T>C ENSP00000354665.2:p.Phe19Leu
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