Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs372261909
- Species
- Homo sapiens
- Symbol
- rs372261909
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SAP30
- Location
- 4:173377313
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.173377313A>G
- HGVS.c name
- ENSEMBL:ENST00000296504.4:c.649A>G
- RefSeq:NM_003864.4:c.649A>G
- HGVS.p name
- ENSP00000296504:p.Ser217Gly
- NP_003855:p.Ser217Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:173369969...173377532 (7.56 kb)
- Assembly version
- Not Available
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