Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199789706
- Species
- Homo sapiens
- Symbol
- rs199789706
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NKRF
- Location
- X:119591267
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- (GRCh38)X:119591267G>A
- HGVS.c name
- ENSEMBL:ENST00000304449.8:c.158C>T
- ENSEMBL:ENST00000371527.1:c.811C>T
- HGVS.p name
- ENSP00000304803:p.Ala53Val
- ENSP00000360582:p.Arg271Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:119588337...119606443 (18.11 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction