Canonical Allele Identifier: CA337099531
Gene: MT-ND5 HGNC NCBI
dbSNP:
2853500
MyVariant.info:
GRCh38 chrMT:g.12720A>G
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12720A>G , J01415.2:m.12720A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.384A>G ENSP00000354813.2:p.Ile128Met
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