Canonical Allele Identifier: CA337099332
Gene: MT-ND4 HGNC NCBI

Linked Data

dbSNP Id: rs878997763
MyVariant Identifiers: chrMT:g.11908A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11908A>G , J01415.2:m.11908A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.1149A>G ENSP00000354961.2:p.Val383=