Canonical Allele Identifier: CA414821531
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693696
ClinVar RCV Id: RCV000855076
dbSNP Id: rs1603224619
MyVariant Identifiers: chrMT:g.14234T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14234T>C , J01415.2:m.14234T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.440A>G ENSP00000354665.2:p.Asp147Gly
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