Canonical Allele Identifier: CA414819424
Gene: MT-ND5 HGNC NCBI

Linked Data

dbSNP Id: rs2068737712
MyVariant Identifiers: chrMT:g.13765C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13765C>T , J01415.2:m.13765C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1429C>T ENSP00000354813.2:p.Pro477Ser
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