Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1424457995
- Species
- Homo sapiens
- Symbol
- rs1424457995
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HNRNPU
- Location
- 1:244856161
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000001.11:g.244856161G>A
- HGVS.c name
- ENSEMBL:ENST00000283179.14:c.1670-3C>T
- ENSEMBL:ENST00000366525.8:n.1526-3C>T
- HGVS.p name
- Not Available
- 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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