Canonical Allele Identifier: CA414817992
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13436C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13436C>G , J01415.2:m.13436C>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1100C>G ENSP00000354813.2:p.Pro367Arg
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