Canonical Allele Identifier: CA337098884
Gene: MT-ND4L HGNC NCBI
dbSNP:
28358280
MyVariant.info:
GRCh38 chrMT:g.10550A>G
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10550A>G , J01415.2:m.10550A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.81A>G ENSP00000354728.1:p.Ile27Met
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