Canonical Allele Identifier: CA414774140
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692419
ClinVar RCV Id: RCV000853729
dbSNP Id: rs1603219286
MyVariant Identifiers: chrMT:g.4079A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4079A>G , J01415.2:m.4079A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.773A>G ENSP00000354687.2:p.Tyr258Cys
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