Canonical Allele Identifier: CA414822458
Gene: MT-ND6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693723
ClinVar RCV Id: RCV000855107
dbSNP Id: rs1556424444
MyVariant Identifiers: chrMT:g.14433C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14433C>T , J01415.2:m.14433C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.241G>A ENSP00000354665.2:p.Ala81Thr
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