Canonical Allele Identifier: CA10581196
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235006
ClinVar RCV Id: RCV000223756 RCV000853676
dbSNP Id: rs876661353
MyVariant Identifiers: chrMT:g.3548T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3548T>C , J01415.2:m.3548T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.242T>C ENSP00000354687.2:p.Ile81Thr
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