Canonical Allele Identifier: CA337096911
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs28393930
MyVariant Identifiers: chrMT:g.4582T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4582T>A , J01415.2:m.4582T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.113T>A ENSP00000355046.4:p.Leu38Gln