Canonical Allele Identifier: CA414818829
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693582
ClinVar RCV Id: RCV000854958
dbSNP Id: rs1556424302
MyVariant Identifiers: chrMT:g.13630A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13630A>G , J01415.2:m.13630A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1294A>G ENSP00000354813.2:p.Thr432Ala
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