Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1680652178
- Species
- Homo sapiens
- Symbol
- rs1680652178
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HNRNPU
- Location
- 1:244855443
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:244855443T>C
- HGVS.c name
- ENSEMBL:ENST00000283179.14:c.2090A>G
- ENSEMBL:ENST00000366525.8:n.1946A>G
- HGVS.p name
- ENSP00000283179:p.Asn697Ser
- ENSP00000393151:p.Asn759Ser
- 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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