ClinGen Allele Registry
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Canonical Allele Identifier:
CA414804927
Gene: MT-ND3
HGNC
NCBI
Linked Data
dbSNP Id:
rs2068721065
MyVariant Identifiers:
chrMT:g.10302A>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.10302A>G , J01415.2:m.10302A>G
GRCh38
Transcript Alleles
HGVS
Amino-acid change
ENST00000361227.2:c.244A>G
ENSP00000355206.2:p.Thr82Ala
Search 100 bp 5'
Search 100 bp 3'