Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1216814236
- Species
- Homo sapiens
- Symbol
- rs1216814236
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SAP30
- Location
- 4:173371244
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000004.12:g.173371244C>T
- HGVS.c name
- ENSEMBL:ENST00000296504.4:c.62C>T
- ENSEMBL:ENST00000725023.1:n.133+490G>A
- HGVS.p name
- ENSP00000296504:p.Ala21Val
- NP_003855:p.Ala21Val
- 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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