Canonical Allele Identifier: CA337099873
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693642
ClinVar RCV Id: RCV000855020
dbSNP Id: rs202081448
MyVariant Identifiers: chrMT:g.13958G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13958G>C , J01415.2:m.13958G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1622G>C ENSP00000354813.2:p.Gly541Ala
Search 100 bp 5'
Search 100 bp 3'