Canonical Allele Identifier: CA337098950
Gene: MT-ND4L HGNC NCBI

Linked Data

dbSNP Id: rs386829109
MyVariant Identifiers: chrMT:g.10679A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10679A>G , J01415.2:m.10679A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.210A>G ENSP00000354728.1:p.Glu70=
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