Canonical Allele Identifier: CA414773965
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1684908
ClinVar RCV Id: RCV002248000
dbSNP Id: rs1603219246
MyVariant Identifiers: chrMT:g.3995A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3995A>G , J01415.2:m.3995A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.689A>G ENSP00000354687.2:p.Asn230Ser
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