Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1419565672
- Species
- Homo sapiens
- Symbol
- rs1419565672
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RETREG1
- Location
- 5:16616957
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000005.10:g.16616957C>A
- HGVS.c name
- ENSEMBL:ENST00000306320.10:c.15G>T
- ENSEMBL:ENST00000499131.1:n.561+471C>A
- HGVS.p name
- ENSP00000304642:p.Ala5=
- ENSP00000507342:p.Ala5=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:16473038...16617101 (144.06 kb)
- Assembly version
- Not Available
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