Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs576563684
- Species
- Homo sapiens
- Symbol
- rs576563684
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CPTP
- Location
- 1:1326921
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.1326921C>T
- HGVS.c name
- ENSEMBL:ENST00000343938.9:c.11C>T
- ENSEMBL:ENST00000464957.1:n.348-320C>T
- HGVS.p name
- ENSP00000343890:p.Ser4Leu
- ENSP00000462636:p.Ser4Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:1324756...1328896 (4.14 kb)
- Assembly version
- Not Available
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