Canonical Allele Identifier: CA337099772
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693592
ClinVar RCV Id: RCV000854969
dbSNP Id: rs386829187
MyVariant Identifiers: chrMT:g.13681A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13681A>T , J01415.2:m.13681A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1345A>T ENSP00000354813.2:p.Thr449Ser
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Search 100 bp 3'