ClinGen Allele Registry
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Canonical Allele Identifier:
CA337100023
Gene: MT-ND6
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.14365C>G
Linked Data - NCBI & NCI
dbSNP:
2853815
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.14365C>G , J01415.2:m.14365C>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361681.2:c.309G>C
ENSP00000354665.2:p.Val103=
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