Canonical Allele Identifier: CA337096558
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692360
ClinVar RCV Id: RCV000853664
dbSNP Id: rs200319905
MyVariant Identifiers: chrMT:g.3497C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3497C>T , J01415.2:m.3497C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.191C>T ENSP00000354687.2:p.Ala64Val
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Search 100 bp 3'