Canonical Allele Identifier: CA337099109
Gene: MT-ND4 HGNC NCBI

Linked Data

dbSNP Id: rs2853490
MyVariant Identifiers: chrMT:g.11176G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11176G>A , J01415.2:m.11176G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.417G>A ENSP00000354961.2:p.Gln139=
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