Canonical Allele Identifier: CA337100003
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693709
ClinVar RCV Id: RCV000855090
dbSNP Id: rs28357675
MyVariant Identifiers: chrMT:g.14318T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14318T>C , J01415.2:m.14318T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361681.2:c.356A>G ENSP00000354665.2:p.Asn119Ser
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