Canonical Allele Identifier: CA414805538
Gene: MT-ND4L HGNC NCBI

Linked Data

ClinVar Variation Id: 693291
ClinVar RCV Id: RCV000854651
dbSNP Id: rs1603222854
MyVariant Identifiers: chrMT:g.10489A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10489A>G , J01415.2:m.10489A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.20A>G ENSP00000354728.1:p.Asn7Ser
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