Canonical Allele Identifier: CA254855
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 9699
ClinVar RCV Id: RCV000010339
dbSNP Id: rs267606894
MyVariant Identifiers: chrMT:g.12770A>G (hg38)
PubMed: PMID:12509858
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12770A>G , J01415.2:m.12770A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.434A>G ENSP00000354813.2:p.Glu145Gly
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Search 100 bp 3'