Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1680217566
- Species
- Homo sapiens
- Symbol
- rs1680217566
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HNRNPU
- Location
- 1:244841961
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- (GRCh38)1:244841961A>G
- HGVS.c name
- ENSEMBL:ENST00000366527.4:n.11529T>C
- ENSEMBL:ENST00000366528.3:c.96A>G
- HGVS.p name
- ENSP00000355486:p.Gly32=
- ENSP00000406327:p.Gly20=
- 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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