Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs144415591
- Species
- Homo sapiens
- Symbol
- rs144415591
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RBKS
- Location
- 2:27827722
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)2:27827722C>T
- HGVS.c name
- ENSEMBL:ENST00000302188.8:c.640G>A
- ENSEMBL:ENST00000448427.1:n.203+45028C>T
- HGVS.p name
- ENSP00000306817:p.Ala214Thr
- ENSP00000393558:p.Arg74His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:27781379...27890681 (109.30 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction