Canonical Allele Identifier: CA414774232
Gene: MT-ND1 HGNC NCBI

Linked Data

dbSNP Id: rs2124592064
MyVariant Identifiers: chrMT:g.4121G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4121G>A , J01415.2:m.4121G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.815G>A ENSP00000354687.2:p.Ter272=