Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs766092096
- Species
- Homo sapiens
- Symbol
- rs766092096
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MDM1
- Location
- 12:68326863
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:68326863C>T
- HGVS.c name
- ENSEMBL:ENST00000303145.11:c.292G>A
- ENSEMBL:ENST00000393543.7:c.*571G>A
- HGVS.p name
- ENSP00000302537:p.Glu98Lys
- ENSP00000391006:p.Glu98Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:68272443...68332381 (59.94 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction