Canonical Allele Identifier: CA337100021
Gene: MT-ND6 HGNC NCBI

Linked Data

dbSNP Id: rs879086798
COSMIC: COSM1155557 COSM1155558
MyVariant Identifiers: chrMT:g.14364G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14364G>A , J01415.2:m.14364G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361681.2:c.310C>T ENSP00000354665.2:p.Leu104=
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