Canonical Allele Identifier: CA414807532
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693330
ClinVar RCV Id: RCV000854692
dbSNP Id: rs1603223021
MyVariant Identifiers: chrMT:g.10922A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10922A>G , J01415.2:m.10922A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.163A>G ENSP00000354961.2:p.Thr55Ala
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