Canonical Allele Identifier: CA414820143
Gene: MT-ND5 HGNC NCBI
dbSNP:
28359184
MyVariant.info:
GRCh38 chrMT:g.13928G>T
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13928G>T , J01415.2:m.13928G>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1592G>T ENSP00000354813.2:p.Ser531Ile
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