Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1668995001
- Species
- Homo sapiens
- Symbol
- rs1668995001
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT61B
- Location
- 2:28849861
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:28849861C>T
- HGVS.c name
- ENSEMBL:ENST00000306108.10:c.*338G>A
- ENSEMBL:ENST00000334056.10:c.862C>T
- HGVS.p name
- ENSP00000335628:p.His288Tyr
- ENSP00000368898:p.His288Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:28849821...28870309 (20.49 kb)
- Assembly version
- Not Available
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