Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1445734357
- Species
- Homo sapiens
- Symbol
- rs1445734357
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HNRNPU
- Location
- 1:244856142
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.244856142T>G
- HGVS.c name
- ENSEMBL:ENST00000283179.14:c.1686A>C
- ENSEMBL:ENST00000366525.8:n.1542A>C
- HGVS.p name
- ENSP00000283179:p.Pro562=
- ENSP00000393151:p.Pro624=
- 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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