Canonical Allele Identifier: CA414773801
Gene: MT-ND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.3919T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3919T>C , J01415.2:m.3919T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.613T>C ENSP00000354687.2:p.Ser205Pro