Canonical Allele Identifier: CA414773176
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692379
ClinVar RCV Id: RCV000853685
dbSNP Id: rs1603219051
MyVariant Identifiers: chrMT:g.3628A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3628A>T , J01415.2:m.3628A>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.322A>T ENSP00000354687.2:p.Thr108Ser
Search 100 bp 5'
Search 100 bp 3'