Canonical Allele Identifier: CA120638
Gene: MT-ND3 HGNC NCBI
ClinVar RCV:
RCV000010359
RCV000854647
ClinVar Variation:
9713
dbSNP:
2853826
MyVariant.info:
GRCh38 chrMT:g.10398A>G
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10398A>G , J01415.2:m.10398A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361227.2:c.340A>G ENSP00000355206.2:p.Thr114Ala
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Search 100 bp 3'