Canonical Allele Identifier: CA414806301
Gene: MT-ND4L HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10666T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10666T>C , J01415.2:m.10666T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.197T>C ENSP00000354728.1:p.Phe66Ser
Search 100 bp 5'
Search 100 bp 3'