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Canonical Allele Identifier:
CA414805411
Gene: MT-ND3
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.10398A>T
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000854648
ClinVar Variation:
693288
dbSNP:
2853826
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.10398A>T , J01415.2:m.10398A>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361227.2:c.340A>T
ENSP00000355206.2:p.Thr114Ser
Search 100 bp 5'
Search 100 bp 3'