Canonical Allele Identifier: CA414774778
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4575A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4575A>T , J01415.2:m.4575A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.106A>T ENSP00000355046.4:p.Asn36Tyr