Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1324125447
- Species
- Homo sapiens
- Symbol
- rs1324125447
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NEFH
- Location
- 22:29480340
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)22:29480340C>T
- HGVS.c name
- ENSEMBL:ENST00000310624.7:c.78C>T
- RefSeq:NM_021076.4:c.78C>T
- HGVS.p name
- ENSP00000311997:p.Tyr26=
- NP_066554:p.Tyr26=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:29480218...29491390 (11.17 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction