Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2102985465
- Species
- Homo sapiens
- Symbol
- rs2102985465
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HNRNPU
- Location
- 1:244856137
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- stop lost
- HGVS.g name
- (GRCh38)1:244856137A>T
- HGVS.c name
- ENSEMBL:ENST00000283179.14:c.1691T>A
- ENSEMBL:ENST00000366525.8:n.1547T>A
- HGVS.p name
- ENSP00000283179:p.Val564Glu
- ENSP00000393151:p.Val626Glu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:244840638...244864560 (23.92 kb)
- Assembly version
- Not Available
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