Canonical Allele Identifier: CA414774174
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692423
ClinVar RCV Id: RCV000853733
dbSNP Id: rs1603219299
MyVariant Identifiers: chrMT:g.4094C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4094C>T , J01415.2:m.4094C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.788C>T ENSP00000354687.2:p.Thr263Ile
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