Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1939992902
- Species
- Homo sapiens
- Symbol
- rs1939992902
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CD96
- Location
- 3:111649714
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.111649714C>T
- HGVS.c name
- ENSEMBL:ENST00000283285.10:c.1666C>T
- ENSEMBL:ENST00000352690.9:c.1618C>T
- HGVS.p name
- ENSP00000283285:p.Pro556Ser
- ENSP00000342040:p.Pro540Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:111292719...111665996 (373.28 kb)
- Assembly version
- Not Available
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