Canonical Allele Identifier: CA414821909
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693708
ClinVar RCV Id: RCV000855089
dbSNP Id: rs1603224668
MyVariant Identifiers: chrMT:g.14315C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14315C>T , J01415.2:m.14315C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.359G>A ENSP00000354665.2:p.Ser120Asn
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