Canonical Allele Identifier: CA337099854
Gene: MT-ND5 HGNC NCBI
ClinVar RCV:
RCV000855014
ClinVar Variation:
693636
dbSNP:
28359184
MyVariant.info:
GRCh38 chrMT:g.13928G>A
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1592G>A ENSP00000354813.2:p.Ser531Asn
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