Canonical Allele Identifier: CA337096899
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs386828945
MyVariant Identifiers: chrMT:g.4541G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4541G>T , J01415.2:m.4541G>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.72G>T ENSP00000355046.4:p.Ser24=