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Canonical Allele Identifier:
CA340947
Gene: MT-ND1
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.3796A>G
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000010382
RCV000853708
RCV000992363
ClinVar Variation:
9730
dbSNP:
28357970
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.3796A>G , J01415.2:m.3796A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361390.2:c.490A>G
ENSP00000354687.2:p.Thr164Ala
Search 100 bp 5'
Search 100 bp 3'