Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs934253899
- Species
- Homo sapiens
- Symbol
- rs934253899
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MANSC4
- Location
- 12:27762920
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:27762920T>C
- HGVS.c name
- ENSEMBL:ENST00000381273.4:c.841A>G
- RefSeq:NM_001146221.5:c.841A>G
- HGVS.p name
- ENSP00000370673:p.Thr281Ala
- NP_001139693:p.Thr281Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:27762427...27780236 (17.81 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction