ClinGen Allele Registry
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Canonical Allele Identifier:
CA414821785
Gene: MT-ND6
HGNC
NCBI
Linked Data
COSMIC:
COSM1155551
COSM1155552
MyVariant Identifiers:
chrMT:g.14291T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.14291T>C , J01415.2:m.14291T>C
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361681.2:c.383A>G
ENSP00000354665.2:p.Glu128Gly
Search 100 bp 5'
Search 100 bp 3'