Canonical Allele Identifier: CA254857
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 9709
ClinVar RCV Id: RCV000010355 RCV000854703
dbSNP Id: rs199476113
MyVariant Identifiers: chrMT:g.11084A>G (hg38)
PubMed: PMID:1323207 PMID:3395302 PMID:8213827
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11084A>G , J01415.2:m.11084A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.325A>G ENSP00000354961.2:p.Thr109Ala
Search 100 bp 5'
Search 100 bp 3'