Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1413692088
- Species
- Homo sapiens
- Symbol
- rs1413692088
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PURA
- Location
- 5:140114602
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- (GRCh38)5:140114602C>A
- HGVS.c name
- ENSEMBL:ENST00000331327.5:c.421C>A
- ENSEMBL:ENST00000520928.2:n.114G>T
- HGVS.p name
- ENSP00000332706:p.Arg141=
- ENSP00000499133:p.Arg141=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:140107777...140125619 (17.84 kb)
- Assembly version
- Not Available
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