Canonical Allele Identifier: CA414804614
Gene: MT-ND3 HGNC NCBI

Linked Data

dbSNP Id: rs193302927
MyVariant Identifiers: chrMT:g.10238T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10238T>C , J01415.2:m.10238T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.180T>C ENSP00000355206.2:p.Ile60=
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