Canonical Allele Identifier: CA414809460
Gene: MT-ND4 HGNC NCBI

Linked Data

dbSNP Id: rs879228903
MyVariant Identifiers: chrMT:g.11101A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11101A>T , J01415.2:m.11101A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.342A>T ENSP00000354961.2:p.Glu114Asp